* About the role * Abcam are looking for a Scientific Product Administrator to support integrating new products into the catalogue and help maintain and enhance our product data. * Roles & Responsibilities * * To contribute to maintaining and enhancing our existing product data through our product updates procedures. * By compiling and checking datasheets ensuring that they contain all information required by customers. * Create kit protocol booklets for kits and assays adhering to guidelines provided by both the project and product managers. * Ensure images received from our partners are analysed and our strict quality standards are upheld. * Participate in team meetings and contribute toward our need to continually improve our processes and product information. * About you * Our ideal candidate will be educated to degree level in a biological science (or equivalent), with good knowledge of antibodies and proteins. Previous experience working in a Life Science company in a similar would be desirable but not essential. You will have an understanding of antibody techniques e.g. western blot, immunohistochemistry, immunocytochemistry, ELISA or flow cytometry. You will also have knowledge of databases such as Uniprot, NCBI and PubMed. You will be highly organised with great time management skills, able to work to deadlines with high attention to detail. You will have excellent communication skills with the ability to work independently and in a team. Competency in MS office applications is a must in this role and experience with Python and SQL would be advantageous but not essential. If this sounds like you and you'd like to be a part of a fast-paced, growing business with the vision to become the most influential company and best-loved brand in life sciences, please apply now! * Pay and Benefits * In addition to competitive salaries, we offer an attractive and flexible benefits package (including our award-winning share scheme, 18 weeks full paid maternity leave and 6 weeks full paid paternity leave), a culture focused on well-being and opportunities for growth and development, and a highly flexible working environment. What's more, as a WORK180 Endorsed Employer, we are recognized globally as an organization that's diverse, inclusive and supports women in the workplace. * About Us * An idea conceived in a University of Cambridge laboratory in 1998, * Abcam plc * * () * began life as an innovative and entrepreneurial start-up, spearheaded by like-minded individuals who shared a common purpose of providing the scientific community with quality antibody reagents, as well as trustworthy and up-to-date information about their uses and limitations. Abcam has now grown to become a leading supplier of protein research tools to life scientists, whilst always maintaining the core collaborative values assumed at its inception. Abcam now supports life science researchers in their quest to understand the cause of disease and ultimately offer improvements to diagnoses and treatments. To achieve this outcome, the company both develops and manufactures its own products in specialist facilities across the globe, and sources from over 400 partners, offering scientists the newest, most innovative and highest quality research tools available globally, regardless of source. With a customer base of research scientists who require high performance products with detailed technical specifications, 64% of global researchers use Abcam products. * Inclusion & Diversity * Abcam is an Equal Opportunity Employer and makes all employment decisions without regard to age, national origin, race, ethnicity, religion, creed, gender, sexual orientation, disability, veteran status, or any other characteristic protected by law.
Dec 03, 2020
Full time
* About the role * Abcam are looking for a Scientific Product Administrator to support integrating new products into the catalogue and help maintain and enhance our product data. * Roles & Responsibilities * * To contribute to maintaining and enhancing our existing product data through our product updates procedures. * By compiling and checking datasheets ensuring that they contain all information required by customers. * Create kit protocol booklets for kits and assays adhering to guidelines provided by both the project and product managers. * Ensure images received from our partners are analysed and our strict quality standards are upheld. * Participate in team meetings and contribute toward our need to continually improve our processes and product information. * About you * Our ideal candidate will be educated to degree level in a biological science (or equivalent), with good knowledge of antibodies and proteins. Previous experience working in a Life Science company in a similar would be desirable but not essential. You will have an understanding of antibody techniques e.g. western blot, immunohistochemistry, immunocytochemistry, ELISA or flow cytometry. You will also have knowledge of databases such as Uniprot, NCBI and PubMed. You will be highly organised with great time management skills, able to work to deadlines with high attention to detail. You will have excellent communication skills with the ability to work independently and in a team. Competency in MS office applications is a must in this role and experience with Python and SQL would be advantageous but not essential. If this sounds like you and you'd like to be a part of a fast-paced, growing business with the vision to become the most influential company and best-loved brand in life sciences, please apply now! * Pay and Benefits * In addition to competitive salaries, we offer an attractive and flexible benefits package (including our award-winning share scheme, 18 weeks full paid maternity leave and 6 weeks full paid paternity leave), a culture focused on well-being and opportunities for growth and development, and a highly flexible working environment. What's more, as a WORK180 Endorsed Employer, we are recognized globally as an organization that's diverse, inclusive and supports women in the workplace. * About Us * An idea conceived in a University of Cambridge laboratory in 1998, * Abcam plc * * () * began life as an innovative and entrepreneurial start-up, spearheaded by like-minded individuals who shared a common purpose of providing the scientific community with quality antibody reagents, as well as trustworthy and up-to-date information about their uses and limitations. Abcam has now grown to become a leading supplier of protein research tools to life scientists, whilst always maintaining the core collaborative values assumed at its inception. Abcam now supports life science researchers in their quest to understand the cause of disease and ultimately offer improvements to diagnoses and treatments. To achieve this outcome, the company both develops and manufactures its own products in specialist facilities across the globe, and sources from over 400 partners, offering scientists the newest, most innovative and highest quality research tools available globally, regardless of source. With a customer base of research scientists who require high performance products with detailed technical specifications, 64% of global researchers use Abcam products. * Inclusion & Diversity * Abcam is an Equal Opportunity Employer and makes all employment decisions without regard to age, national origin, race, ethnicity, religion, creed, gender, sexual orientation, disability, veteran status, or any other characteristic protected by law.
General Store Manager Designate ( Cambridge ) £38,000 - £45,000 + Bonus + Package A fantastic opportunity up for grabs with an extremely iconic Outdoor & Leisure retail brand that are experiencing significant growth & change. If you have larger format Store Management experience within a customer focused business then we want to hear from YOU ! General Store Manager to successfully manage an ...... click apply for full job details
Dec 03, 2020
Full time
General Store Manager Designate ( Cambridge ) £38,000 - £45,000 + Bonus + Package A fantastic opportunity up for grabs with an extremely iconic Outdoor & Leisure retail brand that are experiencing significant growth & change. If you have larger format Store Management experience within a customer focused business then we want to hear from YOU ! General Store Manager to successfully manage an ...... click apply for full job details
Technical Services Manager Recruitment Agency reference: We are currently working with a highly regarded organisation based in Cambridgeshire to help source a Technical Services Manager reporting into the Compliance Programme Manager. We are looking for individuals with a technical skillset and management experience around mechanical, refrigeration, electrical, fire or water...... click apply for full job details
Dec 03, 2020
Contractor
Technical Services Manager Recruitment Agency reference: We are currently working with a highly regarded organisation based in Cambridgeshire to help source a Technical Services Manager reporting into the Compliance Programme Manager. We are looking for individuals with a technical skillset and management experience around mechanical, refrigeration, electrical, fire or water...... click apply for full job details
* About the Role: * The Head of Product Quality will be a role responsible for the strategic direction and delivery of product quality in Abcam, delivering globally through multiple programmes and product platforms. Based in Cambridge, UK, the role holder will be responsible for the implementation of strategy to deliver the highest quality of products to Abcam customers through the professional lab teams. This will be delivered across multiple programme streams advising on the quality required within streams. The role holder will have direct line managerial responsibility for the Product Quality team, and will represent the knockout project delivering key messages around the project within the business and externally at aligned conferences, webinars and events. Additionally, the role holder will drive the operational arm of the complaints team, delivering high quality testing and analysis of complaints and complaint resolution. The role will report to the Director of Antibody Validation and Characterization in Cambridge, UK. This is a leadership position in the New Product Development department and the candidate will be expected to play a leading role in quality discussions globally throughout the business. * Essential duties and responsibilities: * * Implementation of the strategy and delivery of product quality programme in Abcam globally. * Strategic oversight and line managerial responsibility of the Cambridge knockout team and deliverables from the KO project, aligned with the cell lines programme teams. * Oversight and line managerial responsibility of the in-house operational complaints process driving improvements in the scientific quality of complaints testing, turnaround of testing and final quality decision * Representation of the complaints team with Abcam customers with severe complaints. * Contribute to decisions of quality testing and strategic testing of targets for improving quality. * Act as an external expert in quality and reproducibility of abcam products in webinars, conferences and events. * About you: * You have an established track record of strategic thinking and driving high quality performance in teams and in products. You have an eye for detail and a questioning nature to drive the product quality through all our platforms. You will have a wide range of technical experience, including Western Blotting, immunocytochemistry, immunohistochemistry and flow cytometry, as well as an understanding of KO cell line generation. You will enjoy the challenge of a global role which will harness your skills in stakeholder management across the business. If this sounds like you and you'd like to be a part of a fast paced, growing business with the vision to become the most influential company and best-loved brand in life sciences please apply now! * Minimum Qualifications: * * A BS Degree in biochemistry, pathology, cell and molecular biology, immunology or other Life Sciences. * A PhD and post-doctoral experience or equivalent research experience. * Significant experience in driving product specifications and quality. * Experience in leading performance in a fast-paced environment * Experience in pharma, biotech or IVD development businesses is desirable * Experience of flow cytometry, immunohistochemistry, immunocytochemistry and western blotting is desirable. * Demonstrates excellent interpersonal, verbal and written communication skills and excel in cross-functional, collaborative and fast-paced settings. * Knowledge of ISO requirements and familiar with GLP/GMP procedures is preferred. * If this sounds like you and you'd like to be a part of a fast-paced, growing business with the vision to become the most influential company and best-loved brand in life sciences, please apply now! * Pay and Benefits * In addition to competitive salaries, we offer an attractive and flexible benefits package (including our award-winning share scheme, 18 weeks full paid maternity leave and 6 weeks full paid paternity leave), a culture focused on well-being and opportunities for growth and development, and a highly flexible working environment. What's more, as a WORK180 Endorsed Employer, we are recognized globally as an organization that's diverse, inclusive and supports women in the workplace. * About Us * An idea conceived in a University of Cambridge laboratory in 1998, *Abcam plc () *began life as an innovative and entrepreneurial start-up, spearheaded by like-minded individuals who shared a common purpose of providing the scientific community with quality antibody reagents, as well as trustworthy and up-to-date information about their uses and limitations. Abcam has now grown to become a leading supplier of protein research tools to life scientists, whilst always maintaining the core collaborative values assumed at its inception. Abcam now supports life science researchers in their quest to understand the cause of disease and ultimately offer improvements to diagnoses and treatments. To achieve this outcome, the company both develops and manufactures its own products in specialist facilities across the globe, and sources from over 400 partners, offering scientists the newest, most innovative and highest quality research tools available globally, regardless of source. With a customer base of research scientists who require high performance products with detailed technical specifications, 64% of global researchers use Abcam products. * Inclusion & Diversity * Abcam is an Equal Opportunity Employer and makes all employment decisions without regard to age, national origin, race, ethnicity, religion, creed, gender, sexual orientation, disability, veteran status, or any other characteristic protected by law.
Dec 03, 2020
Full time
* About the Role: * The Head of Product Quality will be a role responsible for the strategic direction and delivery of product quality in Abcam, delivering globally through multiple programmes and product platforms. Based in Cambridge, UK, the role holder will be responsible for the implementation of strategy to deliver the highest quality of products to Abcam customers through the professional lab teams. This will be delivered across multiple programme streams advising on the quality required within streams. The role holder will have direct line managerial responsibility for the Product Quality team, and will represent the knockout project delivering key messages around the project within the business and externally at aligned conferences, webinars and events. Additionally, the role holder will drive the operational arm of the complaints team, delivering high quality testing and analysis of complaints and complaint resolution. The role will report to the Director of Antibody Validation and Characterization in Cambridge, UK. This is a leadership position in the New Product Development department and the candidate will be expected to play a leading role in quality discussions globally throughout the business. * Essential duties and responsibilities: * * Implementation of the strategy and delivery of product quality programme in Abcam globally. * Strategic oversight and line managerial responsibility of the Cambridge knockout team and deliverables from the KO project, aligned with the cell lines programme teams. * Oversight and line managerial responsibility of the in-house operational complaints process driving improvements in the scientific quality of complaints testing, turnaround of testing and final quality decision * Representation of the complaints team with Abcam customers with severe complaints. * Contribute to decisions of quality testing and strategic testing of targets for improving quality. * Act as an external expert in quality and reproducibility of abcam products in webinars, conferences and events. * About you: * You have an established track record of strategic thinking and driving high quality performance in teams and in products. You have an eye for detail and a questioning nature to drive the product quality through all our platforms. You will have a wide range of technical experience, including Western Blotting, immunocytochemistry, immunohistochemistry and flow cytometry, as well as an understanding of KO cell line generation. You will enjoy the challenge of a global role which will harness your skills in stakeholder management across the business. If this sounds like you and you'd like to be a part of a fast paced, growing business with the vision to become the most influential company and best-loved brand in life sciences please apply now! * Minimum Qualifications: * * A BS Degree in biochemistry, pathology, cell and molecular biology, immunology or other Life Sciences. * A PhD and post-doctoral experience or equivalent research experience. * Significant experience in driving product specifications and quality. * Experience in leading performance in a fast-paced environment * Experience in pharma, biotech or IVD development businesses is desirable * Experience of flow cytometry, immunohistochemistry, immunocytochemistry and western blotting is desirable. * Demonstrates excellent interpersonal, verbal and written communication skills and excel in cross-functional, collaborative and fast-paced settings. * Knowledge of ISO requirements and familiar with GLP/GMP procedures is preferred. * If this sounds like you and you'd like to be a part of a fast-paced, growing business with the vision to become the most influential company and best-loved brand in life sciences, please apply now! * Pay and Benefits * In addition to competitive salaries, we offer an attractive and flexible benefits package (including our award-winning share scheme, 18 weeks full paid maternity leave and 6 weeks full paid paternity leave), a culture focused on well-being and opportunities for growth and development, and a highly flexible working environment. What's more, as a WORK180 Endorsed Employer, we are recognized globally as an organization that's diverse, inclusive and supports women in the workplace. * About Us * An idea conceived in a University of Cambridge laboratory in 1998, *Abcam plc () *began life as an innovative and entrepreneurial start-up, spearheaded by like-minded individuals who shared a common purpose of providing the scientific community with quality antibody reagents, as well as trustworthy and up-to-date information about their uses and limitations. Abcam has now grown to become a leading supplier of protein research tools to life scientists, whilst always maintaining the core collaborative values assumed at its inception. Abcam now supports life science researchers in their quest to understand the cause of disease and ultimately offer improvements to diagnoses and treatments. To achieve this outcome, the company both develops and manufactures its own products in specialist facilities across the globe, and sources from over 400 partners, offering scientists the newest, most innovative and highest quality research tools available globally, regardless of source. With a customer base of research scientists who require high performance products with detailed technical specifications, 64% of global researchers use Abcam products. * Inclusion & Diversity * Abcam is an Equal Opportunity Employer and makes all employment decisions without regard to age, national origin, race, ethnicity, religion, creed, gender, sexual orientation, disability, veteran status, or any other characteristic protected by law.
Please note: All our collections are currently taking place online Our bucket collectors are amazing- and now they're going virtual! Can you give up your time to help raise money for people in crisis and are the power of kindness in your community. To join our team you don't need any previous experience. We only ask that you are warm and enthusiastic, and willing to share your virtual bucket collection with your friends, family and other contacts. You will need to be over 16 (16-17 subject to parental consent, risk assessment and supervisory considerations). We look forward to meeting you! Covid19 health and safety statement We can now accept applications from people who are clinically extremely vulnerable or clinically vulnerable. Deployment into role with be subject to government guidelines and individual and building risk assessments. More about this role Volunteer role Fundraising bucket shaker volunteer Volunteer manager Fundraising manager Where you will be based Community Why we want you A few hours of your time collecting with us could raise enough cash to change people's lives. For example: £5 could buy a food parcel in Mongolia £8 could buy three mosquito nets in Sierra Leone £10 could buy 30 foil blankets for people in crisis in the UK £20 could help buy emergency food supplies for a family of 4 during a crisis in the UK There are British Red Cross collections taking place all year, online and face to face where appropriate. What you will be doing Meet at a pre-arranged location such as a supermarket, station or other public place Shake your bucket (for real or online!) Have fun! The skills you need Warm and friendly Free for a couple of hours? Minimum age 16 (subject to parental consent, risk assessment and safeguarding considerations) What's in it for you Help people in crisis at home and abroad Gain experience and confidence Be the power of kindness in your community
Dec 03, 2020
Full time
Please note: All our collections are currently taking place online Our bucket collectors are amazing- and now they're going virtual! Can you give up your time to help raise money for people in crisis and are the power of kindness in your community. To join our team you don't need any previous experience. We only ask that you are warm and enthusiastic, and willing to share your virtual bucket collection with your friends, family and other contacts. You will need to be over 16 (16-17 subject to parental consent, risk assessment and supervisory considerations). We look forward to meeting you! Covid19 health and safety statement We can now accept applications from people who are clinically extremely vulnerable or clinically vulnerable. Deployment into role with be subject to government guidelines and individual and building risk assessments. More about this role Volunteer role Fundraising bucket shaker volunteer Volunteer manager Fundraising manager Where you will be based Community Why we want you A few hours of your time collecting with us could raise enough cash to change people's lives. For example: £5 could buy a food parcel in Mongolia £8 could buy three mosquito nets in Sierra Leone £10 could buy 30 foil blankets for people in crisis in the UK £20 could help buy emergency food supplies for a family of 4 during a crisis in the UK There are British Red Cross collections taking place all year, online and face to face where appropriate. What you will be doing Meet at a pre-arranged location such as a supermarket, station or other public place Shake your bucket (for real or online!) Have fun! The skills you need Warm and friendly Free for a couple of hours? Minimum age 16 (subject to parental consent, risk assessment and safeguarding considerations) What's in it for you Help people in crisis at home and abroad Gain experience and confidence Be the power of kindness in your community
My client are a market leading provider of innovative Geospatial solutions and services; financially sound and continuing to grow through success, they're looking to expand their professional services team to meet growth plans for next year. The Role Our Project Managers are responsible for the successful planning and delivery of projects across our diverse set of customers and industry sectors...... click apply for full job details
Dec 03, 2020
Full time
My client are a market leading provider of innovative Geospatial solutions and services; financially sound and continuing to grow through success, they're looking to expand their professional services team to meet growth plans for next year. The Role Our Project Managers are responsible for the successful planning and delivery of projects across our diverse set of customers and industry sectors...... click apply for full job details
Office For National Statistics
Cambridge, Cambridgeshire
Communal establishments officers 25 hours a week Contract: 16 February 2021 to 14 April 2021 plus holiday Salary dependent on location Band 1 - £14.61 Band 2 - £12.64 Band 3 - £11.22 No fixed daily working hours but you must work within the following times: Monday to Saturday: 9am and 8pm Sundays and bank holidays: 10am and 4pm Confident communicators make the census The census is a survey of the entire population of England and Wales that happens every 10 years. It's run by the Office for National Statistics (ONS) and gives us a picture of all the people and households in England and Wales. The information we collect is used to make decisions that affect everyone - things like how many schools, surgeries and hospitals we need. To help us, we need a field team to encourage people in communal establishments (CEs) to take part. CEs are managed residential accommodations such as universities and care homes, so you will meet people from all walks of life. The role In this flexible, temporary role, you will make contact with and visit addresses of CEs, to either deliver or follow up on census questionnaires. Most of your work will be face-to-face, but you will need to make phone calls ahead of some visits, building relationships with accommodation managers and residents to encourage them to take part. You will also help people overcome any objections or barriers to completing the questionnaire either by assisting them yourself or referring them to available support. You will work in a team with assistance and guidance from your team leader, who will meet with you when you are working to help you settle into your role. Your hours will be flexible to help you maximise engagement with the CE populations you need to reach. About you You are an outgoing, confident communicator and you are at ease using smartphones and tablets. You likely have previous customer service experience, and you will be comfortable speaking to members of the public in their own homes. A team player, you are professional and calm in challenging situations. You will be out and about visiting addresses, so you must be prepared to travel. You will need a current, full UK driving license and use of a motor vehicle, insured for business use. We will pay travel expenses within your work area. For roles in Wales, knowledge of Welsh would be an advantage. To be considered for the role, you must be available from 16 February 2020 to 14 April 2021 inclusive. You will also need to be flexible with your hours, because you might have to work evenings and weekends, depending on the accommodation you are visiting. People make the census. If you are comfortable interacting with the public and interested in making Census 2021 a success for everyone, apply for a communal establishments officer role. We can only employ you if you are eligible to work for the Civil Service. Find out more about the Civil Service nationality rules . COVID-19 Your health, and that of our field staff, is very important to us. We will be following the government's safety guidelines about the coronavirus (COVID-19). Appropriate PPE (Personal Protective Equipment) will be provided to all staff. Social distancing will be maintained throughout the operation.
Dec 02, 2020
Full time
Communal establishments officers 25 hours a week Contract: 16 February 2021 to 14 April 2021 plus holiday Salary dependent on location Band 1 - £14.61 Band 2 - £12.64 Band 3 - £11.22 No fixed daily working hours but you must work within the following times: Monday to Saturday: 9am and 8pm Sundays and bank holidays: 10am and 4pm Confident communicators make the census The census is a survey of the entire population of England and Wales that happens every 10 years. It's run by the Office for National Statistics (ONS) and gives us a picture of all the people and households in England and Wales. The information we collect is used to make decisions that affect everyone - things like how many schools, surgeries and hospitals we need. To help us, we need a field team to encourage people in communal establishments (CEs) to take part. CEs are managed residential accommodations such as universities and care homes, so you will meet people from all walks of life. The role In this flexible, temporary role, you will make contact with and visit addresses of CEs, to either deliver or follow up on census questionnaires. Most of your work will be face-to-face, but you will need to make phone calls ahead of some visits, building relationships with accommodation managers and residents to encourage them to take part. You will also help people overcome any objections or barriers to completing the questionnaire either by assisting them yourself or referring them to available support. You will work in a team with assistance and guidance from your team leader, who will meet with you when you are working to help you settle into your role. Your hours will be flexible to help you maximise engagement with the CE populations you need to reach. About you You are an outgoing, confident communicator and you are at ease using smartphones and tablets. You likely have previous customer service experience, and you will be comfortable speaking to members of the public in their own homes. A team player, you are professional and calm in challenging situations. You will be out and about visiting addresses, so you must be prepared to travel. You will need a current, full UK driving license and use of a motor vehicle, insured for business use. We will pay travel expenses within your work area. For roles in Wales, knowledge of Welsh would be an advantage. To be considered for the role, you must be available from 16 February 2020 to 14 April 2021 inclusive. You will also need to be flexible with your hours, because you might have to work evenings and weekends, depending on the accommodation you are visiting. People make the census. If you are comfortable interacting with the public and interested in making Census 2021 a success for everyone, apply for a communal establishments officer role. We can only employ you if you are eligible to work for the Civil Service. Find out more about the Civil Service nationality rules . COVID-19 Your health, and that of our field staff, is very important to us. We will be following the government's safety guidelines about the coronavirus (COVID-19). Appropriate PPE (Personal Protective Equipment) will be provided to all staff. Social distancing will be maintained throughout the operation.
We're looking for amazing videographers to take on clients locally. Are you skilled in your craft, friendly and professional? Are you looking for new clients? If this sounds like you, we'd love to hear from you. Who are we looking for? We want creative and professional videographers who are passionate about the quality of their work. Projects may include parties, exhibitions, family gatherings, corporate events and more, but we encourage our photographers to work within their speciality. If you are happy to liaise and work directly with clients and you have availability to take on more clients, please get in touch.
Dec 02, 2020
Full time
We're looking for amazing videographers to take on clients locally. Are you skilled in your craft, friendly and professional? Are you looking for new clients? If this sounds like you, we'd love to hear from you. Who are we looking for? We want creative and professional videographers who are passionate about the quality of their work. Projects may include parties, exhibitions, family gatherings, corporate events and more, but we encourage our photographers to work within their speciality. If you are happy to liaise and work directly with clients and you have availability to take on more clients, please get in touch.
* About the Role: * The Director of Strategy for Neuroscience at Abcam is a high profile, leadership role responsible for driving Abcam's short and long range commercial and marketing strategies for its portfolio of both inhouse developed and externally sourced neuroscience products across a range of product categories. Your goal is to identify the unmet needs of end users across all of Abcam's customer segments and launch market leading solutions to rapidly resolve these needs. Line managing an established team of 2, the role is responsible for driving understanding of the strengths and opportunities within the existing neuroscience portfolio, understanding the market both now and its future direction along with the needs of Abcam's consumers, as well as understanding and fully utilising inhouse product development capabilities, collaborating with the R&D team to identify opportunities to expand on these capabilities, and with the Commercial and Business Development teams to develop broad consumer partnerships. * About the Research Area Strategy Team: * The Research Area Strategy Team are a highly committed, enthusiastic and ambitious team, focused on collaborative working, innovation and strategic thinking, who thrive on the challenge of achieving stretching goals. The team work in a fast-paced environment where they take a solution first approach to problem solving and are very results focused, with a strong sense of accountability for achieving their goals. What's more, they have a strong sense of fun and energy. * Roles & responsibilities: * Strategic planning: * Following thorough review of the recommendations made by the team, decide on the definition and most appropriate tactics for the execution of the commercial strategy to deliver a step change in revenue growth of the neuroscience product portfolio and achieve challenging annual revenue and margin targets. * Make recommendations into the development of the inhouse R&D pipeline, covering new product types and platforms as well as existing. Commercial analytics * Continually analyse the neuroscience field and provide insight to proactively support the development and execution of the commercial strategy. * Decide which key products and customers to target to develop partnerships that enhance Abcam's global reputation as a leading partner in neuroscience research. Commercial operations: * Recommend the development of new pricing initiatives for the neuroscience portfolio. * Make recommendations into the development of product datasheets and protocols specifically for the neuroscience product range. * Drive the development of the quality criteria required for the neuroscience portfolio. External partnerships: * Make recommendations on inbound and outbound product collaboration opportunities for follow up by the Portfolio Development, Business Development and Custom Products & Licensing teams. * Make decisions on which candidates should form Abcam's external network of scientific advisors in the field. Develop and maintain relationships with these advisors. * Develop and deliver impactful presentations to key external audiences on Abcam's capabilities in neuroscience research to support and input into the process of external engagement for inbound and outbound partnership opportunities. Internal communications: * Develop highly collaborative relationships across all global departments and provide recommendations into new commercial opportunities to deliver the neuroscience strategy and revenue growth. * Represent the voice of the global neuroscience consumer and market across the business. * About you * You will be able to demonstrate significant (at least 10 years) leadership experience in business development in the Biotech/Pharma or Diagnostics industry (ideally also significant experience in sales and marketing). In addition, you will have extensive experience of closing commercial deals. You will preferably have experience in all approaches to antibody development and antibody applications. You will hold a minimum of a BSc in biological sciences or equivalent, a PhD would be advantageous. A background in neuroscience research would be a distinct advantage. You will have proven ability to establish strong working relationships internally and externally. Strong analytical skills and the ability to communicate and present findings and recommendations effectively at a senior level will be key to this role. If this sounds like you and you'd like to be a part of a fast paced, growing business with the vision to become the most influential company and best-loved brand in life sciences please apply now! * *About Us* * An idea conceived in a University of Cambridge laboratory in 1998, * Abcam plc ** ** () ** * began life as an innovative and entrepreneurial start-up, spearheaded by like-minded individuals who shared a common purpose of providing the scientific community with quality antibody reagents, as well as trustworthy and up-to-date information about their uses and limitations. Abcam has now grown to become a leading supplier of protein research tools to life scientists, whilst always maintaining the core collaborative values assumed at its inception. Abcam now supports life science researchers in their quest to understand the cause of disease and ultimately offer improvements to diagnoses and treatments. To achieve this outcome, the company both develops and manufactures its own products in specialist facilities across the globe, and sources from over 400 partners, offering scientists the newest, most innovative and highest quality research tools available globally, regardless of source. With a customer base of research scientists who require high performance products with detailed technical specifications, 64% of global researchers use Abcam products. * Inclusion & Diversity * Abcam is an Equal Opportunity Employer and makes all employment decisions without regard to age, national origin, race, ethnicity, religion, creed, gender, sexual orientation, disability, veteran status, or any other characteristic protected by law.
Dec 02, 2020
Full time
* About the Role: * The Director of Strategy for Neuroscience at Abcam is a high profile, leadership role responsible for driving Abcam's short and long range commercial and marketing strategies for its portfolio of both inhouse developed and externally sourced neuroscience products across a range of product categories. Your goal is to identify the unmet needs of end users across all of Abcam's customer segments and launch market leading solutions to rapidly resolve these needs. Line managing an established team of 2, the role is responsible for driving understanding of the strengths and opportunities within the existing neuroscience portfolio, understanding the market both now and its future direction along with the needs of Abcam's consumers, as well as understanding and fully utilising inhouse product development capabilities, collaborating with the R&D team to identify opportunities to expand on these capabilities, and with the Commercial and Business Development teams to develop broad consumer partnerships. * About the Research Area Strategy Team: * The Research Area Strategy Team are a highly committed, enthusiastic and ambitious team, focused on collaborative working, innovation and strategic thinking, who thrive on the challenge of achieving stretching goals. The team work in a fast-paced environment where they take a solution first approach to problem solving and are very results focused, with a strong sense of accountability for achieving their goals. What's more, they have a strong sense of fun and energy. * Roles & responsibilities: * Strategic planning: * Following thorough review of the recommendations made by the team, decide on the definition and most appropriate tactics for the execution of the commercial strategy to deliver a step change in revenue growth of the neuroscience product portfolio and achieve challenging annual revenue and margin targets. * Make recommendations into the development of the inhouse R&D pipeline, covering new product types and platforms as well as existing. Commercial analytics * Continually analyse the neuroscience field and provide insight to proactively support the development and execution of the commercial strategy. * Decide which key products and customers to target to develop partnerships that enhance Abcam's global reputation as a leading partner in neuroscience research. Commercial operations: * Recommend the development of new pricing initiatives for the neuroscience portfolio. * Make recommendations into the development of product datasheets and protocols specifically for the neuroscience product range. * Drive the development of the quality criteria required for the neuroscience portfolio. External partnerships: * Make recommendations on inbound and outbound product collaboration opportunities for follow up by the Portfolio Development, Business Development and Custom Products & Licensing teams. * Make decisions on which candidates should form Abcam's external network of scientific advisors in the field. Develop and maintain relationships with these advisors. * Develop and deliver impactful presentations to key external audiences on Abcam's capabilities in neuroscience research to support and input into the process of external engagement for inbound and outbound partnership opportunities. Internal communications: * Develop highly collaborative relationships across all global departments and provide recommendations into new commercial opportunities to deliver the neuroscience strategy and revenue growth. * Represent the voice of the global neuroscience consumer and market across the business. * About you * You will be able to demonstrate significant (at least 10 years) leadership experience in business development in the Biotech/Pharma or Diagnostics industry (ideally also significant experience in sales and marketing). In addition, you will have extensive experience of closing commercial deals. You will preferably have experience in all approaches to antibody development and antibody applications. You will hold a minimum of a BSc in biological sciences or equivalent, a PhD would be advantageous. A background in neuroscience research would be a distinct advantage. You will have proven ability to establish strong working relationships internally and externally. Strong analytical skills and the ability to communicate and present findings and recommendations effectively at a senior level will be key to this role. If this sounds like you and you'd like to be a part of a fast paced, growing business with the vision to become the most influential company and best-loved brand in life sciences please apply now! * *About Us* * An idea conceived in a University of Cambridge laboratory in 1998, * Abcam plc ** ** () ** * began life as an innovative and entrepreneurial start-up, spearheaded by like-minded individuals who shared a common purpose of providing the scientific community with quality antibody reagents, as well as trustworthy and up-to-date information about their uses and limitations. Abcam has now grown to become a leading supplier of protein research tools to life scientists, whilst always maintaining the core collaborative values assumed at its inception. Abcam now supports life science researchers in their quest to understand the cause of disease and ultimately offer improvements to diagnoses and treatments. To achieve this outcome, the company both develops and manufactures its own products in specialist facilities across the globe, and sources from over 400 partners, offering scientists the newest, most innovative and highest quality research tools available globally, regardless of source. With a customer base of research scientists who require high performance products with detailed technical specifications, 64% of global researchers use Abcam products. * Inclusion & Diversity * Abcam is an Equal Opportunity Employer and makes all employment decisions without regard to age, national origin, race, ethnicity, religion, creed, gender, sexual orientation, disability, veteran status, or any other characteristic protected by law.
Job Family: Support Worker Location: Cambridge, Cambridgeshire Pay Rate (£): £9.04 per hour Vacancy Reference: 025451 Experienced Support Workers Suez Road, CB1 Full/Part Time Available Full driving licence essential Offering up to £1,422 per month Join us to help provide the best care possible to individuals with learning disabilities to live the most independent and fulfilled lives that we can support. Working with Voyage Care you will receive full training, competitive benefits packages, supported career progression and a great team. Suez Road is 2 properties supporting individuals with living their lives on a daily basis. Each individual at Suez Road that we support has their own unique personality and when able they are all actively out in the community taking part in a variety of different activities such as swimming and going to the cinema. This position is full/part time, covering shifts throughout the week and some nights on a rotational shift basis (0, 1 & 2). We truly believe that by helping individuals with the everyday challenges of washing, dressing, eating and regular activities, that you'll enable them to do the things that most people take for granted. This is a fantastic opportunity to join a growing organisation who truly put those we support at the heart of our business. COVID19 safety is important to us all, we support our staff and the people we support to stay safe by wearing correct PPE, including Type IIR Fluid Resistant Surgical Masks (FRSM), aprons and gloves at all times. We have a in-house team that ensures that all of our services have plenty of PPE at all times. All care and support is carried out following the latest Government guidance. Our aim is to keep you and the people we support safe. If you are interested in this role and would like to find out more, please contact Shane on or click apply. Benefits: We invest in a wide range of benefits to reward our Support Workers for the brilliant job they do. We offer a pension scheme; retail discount package with some great offers, including holiday discounts to gym membership; our employee assistance programme offers independent advice and support 24 hours a day. About Voyage Care: We are passionate about caring for our people. You'll be working with a company that is renowned for treating people properly and providing a training, development, compliance and support structure that simply can't be found anywhere else. We are committed to delivering quality care and that's why our care homes have a quality score of 96%, practically unheard of in our industry. As part of a passionate, close-knit team there will always be someone on hand to help you out. To be part of our Voyage Care family, please click to apply via email or give us a call on We are committed to safeguarding and promoting the welfare of the people we support. All successful candidates will be subject to an Enhanced DBS/PVG check and Regulated Activity which will include a check against the Barred adult list. * Some of our roles require male or female employees only, where this is indicated it is a genuine occupational requirement, in accordance with the Equality Act 2010 Role Specific Requirements - Driver: Driver Required Gender: No Specific Requirement
Dec 02, 2020
Full time
Job Family: Support Worker Location: Cambridge, Cambridgeshire Pay Rate (£): £9.04 per hour Vacancy Reference: 025451 Experienced Support Workers Suez Road, CB1 Full/Part Time Available Full driving licence essential Offering up to £1,422 per month Join us to help provide the best care possible to individuals with learning disabilities to live the most independent and fulfilled lives that we can support. Working with Voyage Care you will receive full training, competitive benefits packages, supported career progression and a great team. Suez Road is 2 properties supporting individuals with living their lives on a daily basis. Each individual at Suez Road that we support has their own unique personality and when able they are all actively out in the community taking part in a variety of different activities such as swimming and going to the cinema. This position is full/part time, covering shifts throughout the week and some nights on a rotational shift basis (0, 1 & 2). We truly believe that by helping individuals with the everyday challenges of washing, dressing, eating and regular activities, that you'll enable them to do the things that most people take for granted. This is a fantastic opportunity to join a growing organisation who truly put those we support at the heart of our business. COVID19 safety is important to us all, we support our staff and the people we support to stay safe by wearing correct PPE, including Type IIR Fluid Resistant Surgical Masks (FRSM), aprons and gloves at all times. We have a in-house team that ensures that all of our services have plenty of PPE at all times. All care and support is carried out following the latest Government guidance. Our aim is to keep you and the people we support safe. If you are interested in this role and would like to find out more, please contact Shane on or click apply. Benefits: We invest in a wide range of benefits to reward our Support Workers for the brilliant job they do. We offer a pension scheme; retail discount package with some great offers, including holiday discounts to gym membership; our employee assistance programme offers independent advice and support 24 hours a day. About Voyage Care: We are passionate about caring for our people. You'll be working with a company that is renowned for treating people properly and providing a training, development, compliance and support structure that simply can't be found anywhere else. We are committed to delivering quality care and that's why our care homes have a quality score of 96%, practically unheard of in our industry. As part of a passionate, close-knit team there will always be someone on hand to help you out. To be part of our Voyage Care family, please click to apply via email or give us a call on We are committed to safeguarding and promoting the welfare of the people we support. All successful candidates will be subject to an Enhanced DBS/PVG check and Regulated Activity which will include a check against the Barred adult list. * Some of our roles require male or female employees only, where this is indicated it is a genuine occupational requirement, in accordance with the Equality Act 2010 Role Specific Requirements - Driver: Driver Required Gender: No Specific Requirement
We are looking for Residential Care Workers to join our amazing team at one of our well-established homes located in Cambridge. The ideal candidate will be confident, passionate and resilient. Previous experience is advantageous and qualifications desirable but not essential. All the children in our care have been victims or at risk of child sexual abuse, trauma or exploitation...... click apply for full job details
Dec 02, 2020
Full time
We are looking for Residential Care Workers to join our amazing team at one of our well-established homes located in Cambridge. The ideal candidate will be confident, passionate and resilient. Previous experience is advantageous and qualifications desirable but not essential. All the children in our care have been victims or at risk of child sexual abuse, trauma or exploitation...... click apply for full job details
Graduate Software Engineer / Developer - Infrastructure Development A unique opportunity for a talented Graduate Software Engineer / Developer, to join an industry-leading software company in Cambridge offering the opportunity to work on a wide variety of internal infrastructure development projects using a diverse toolset...... click apply for full job details
Dec 02, 2020
Full time
Graduate Software Engineer / Developer - Infrastructure Development A unique opportunity for a talented Graduate Software Engineer / Developer, to join an industry-leading software company in Cambridge offering the opportunity to work on a wide variety of internal infrastructure development projects using a diverse toolset...... click apply for full job details
Job Family: Support Worker Location: Cambridge, Cambridgeshire Pay Rate (£): £9.04 per hour Vacancy Reference: 025451 Experienced Support Workers Suez Road, CB1 Full/Part Time Available Full driving licence essential Offering up to £1,422 per month Join us to help provide the best care possible to individuals with learning disabilities to live the most independent and fulfilled lives that we can support. Working with Voyage Care you will receive full training, competitive benefits packages, supported career progression and a great team. Suez Road is 2 properties supporting individuals with living their lives on a daily basis. Each individual at Suez Road that we support has their own unique personality and when able they are all actively out in the community taking part in a variety of different activities such as swimming and going to the cinema. This position is full/part time, covering shifts throughout the week and some nights on a rotational shift basis (0, 1 & 2). We truly believe that by helping individuals with the everyday challenges of washing, dressing, eating and regular activities, that you'll enable them to do the things that most people take for granted. This is a fantastic opportunity to join a growing organisation who truly put those we support at the heart of our business. COVID19 safety is important to us all, we support our staff and the people we support to stay safe by wearing correct PPE, including Type IIR Fluid Resistant Surgical Masks (FRSM), aprons and gloves at all times. We have a in-house team that ensures that all of our services have plenty of PPE at all times. All care and support is carried out following the latest Government guidance. Our aim is to keep you and the people we support safe. If you are interested in this role and would like to find out more, please contact Shane on or click apply. Benefits: We invest in a wide range of benefits to reward our Support Workers for the brilliant job they do. We offer a pension scheme; retail discount package with some great offers, including holiday discounts to gym membership; our employee assistance programme offers independent advice and support 24 hours a day. About Voyage Care: We are passionate about caring for our people. You'll be working with a company that is renowned for treating people properly and providing a training, development, compliance and support structure that simply can't be found anywhere else. We are committed to delivering quality care and that's why our care homes have a quality score of 96%, practically unheard of in our industry. As part of a passionate, close-knit team there will always be someone on hand to help you out. To be part of our Voyage Care family, please click to apply via email or give us a call on We are committed to safeguarding and promoting the welfare of the people we support. All successful candidates will be subject to an Enhanced DBS/PVG check and Regulated Activity which will include a check against the Barred adult list. * Some of our roles require male or female employees only, where this is indicated it is a genuine occupational requirement, in accordance with the Equality Act 2010 Role Specific Requirements - Driver: Driver Required Gender: No Specific Requirement
Dec 02, 2020
Full time
Job Family: Support Worker Location: Cambridge, Cambridgeshire Pay Rate (£): £9.04 per hour Vacancy Reference: 025451 Experienced Support Workers Suez Road, CB1 Full/Part Time Available Full driving licence essential Offering up to £1,422 per month Join us to help provide the best care possible to individuals with learning disabilities to live the most independent and fulfilled lives that we can support. Working with Voyage Care you will receive full training, competitive benefits packages, supported career progression and a great team. Suez Road is 2 properties supporting individuals with living their lives on a daily basis. Each individual at Suez Road that we support has their own unique personality and when able they are all actively out in the community taking part in a variety of different activities such as swimming and going to the cinema. This position is full/part time, covering shifts throughout the week and some nights on a rotational shift basis (0, 1 & 2). We truly believe that by helping individuals with the everyday challenges of washing, dressing, eating and regular activities, that you'll enable them to do the things that most people take for granted. This is a fantastic opportunity to join a growing organisation who truly put those we support at the heart of our business. COVID19 safety is important to us all, we support our staff and the people we support to stay safe by wearing correct PPE, including Type IIR Fluid Resistant Surgical Masks (FRSM), aprons and gloves at all times. We have a in-house team that ensures that all of our services have plenty of PPE at all times. All care and support is carried out following the latest Government guidance. Our aim is to keep you and the people we support safe. If you are interested in this role and would like to find out more, please contact Shane on or click apply. Benefits: We invest in a wide range of benefits to reward our Support Workers for the brilliant job they do. We offer a pension scheme; retail discount package with some great offers, including holiday discounts to gym membership; our employee assistance programme offers independent advice and support 24 hours a day. About Voyage Care: We are passionate about caring for our people. You'll be working with a company that is renowned for treating people properly and providing a training, development, compliance and support structure that simply can't be found anywhere else. We are committed to delivering quality care and that's why our care homes have a quality score of 96%, practically unheard of in our industry. As part of a passionate, close-knit team there will always be someone on hand to help you out. To be part of our Voyage Care family, please click to apply via email or give us a call on We are committed to safeguarding and promoting the welfare of the people we support. All successful candidates will be subject to an Enhanced DBS/PVG check and Regulated Activity which will include a check against the Barred adult list. * Some of our roles require male or female employees only, where this is indicated it is a genuine occupational requirement, in accordance with the Equality Act 2010 Role Specific Requirements - Driver: Driver Required Gender: No Specific Requirement
Salary : up to £34,000 ( dependant on relevant qualifications and experience) I am working for East Anglia's premier boiler and heating experts. We have new opportunities for qualified electricians to join their small, friendly building maintenance and electrical team which is expanding due to continued growth. As an integral part of the team you will undertake domestic and commercial heating installations and repairs, including solar and the latest renewable technologies. You will also carry out EICR testing of domestic and commercial properties and remedial works to bring installations in line with current standards, which includes, but is not limited to, consumer unit replacements and full/partial rewires. You will work Monday to Friday, 8-5pm with an unpaid lunch break of 1 hour. There is the opportunity for call-out if desired. As the ideal candidate you will have experience in general electrical installation work in both domestic and commercial properties. You will be a highly competent professional who takes pride in their job, demonstrate initiative in a varied role, and possess excellent customer service skills. To be considered for this role, we are looking for the following criteria: Essential : NVQ Level 3 in Electrical Installation; 18th Edition of BS7671; Experience of working in domestic properties; Experience in domestic and commercial heating systems; Good understanding and knowledge of Health & Safety in the workplace; Effective communication skills ; Ability to work autonomously as well as part of a successful team; Full UK driving license Desirable : Inspection and Testing Qualification (2391 or 2394/2395) Experience of undertaking Electrical Inspection, Testing and remedial works JIB Gold Card It is a great place to work and this role will provide you with the opportunity to develop your skills and qualifications and as a result, enhance your career. Tools will be provided to successfully perform in your role, such as a company vehicle, full company uniform, tablet and mobile. In return for your commitment they offer an excellent competitive salary and benefits package such as: pension scheme; free platinum boiler cover; discounts from many different retailers, 22 days holiday plus bank holidays ( increasing with length of service ); opportunity to buy and sell holiday; life insurance; life assurance scheme and company sick pay.
Dec 02, 2020
Full time
Salary : up to £34,000 ( dependant on relevant qualifications and experience) I am working for East Anglia's premier boiler and heating experts. We have new opportunities for qualified electricians to join their small, friendly building maintenance and electrical team which is expanding due to continued growth. As an integral part of the team you will undertake domestic and commercial heating installations and repairs, including solar and the latest renewable technologies. You will also carry out EICR testing of domestic and commercial properties and remedial works to bring installations in line with current standards, which includes, but is not limited to, consumer unit replacements and full/partial rewires. You will work Monday to Friday, 8-5pm with an unpaid lunch break of 1 hour. There is the opportunity for call-out if desired. As the ideal candidate you will have experience in general electrical installation work in both domestic and commercial properties. You will be a highly competent professional who takes pride in their job, demonstrate initiative in a varied role, and possess excellent customer service skills. To be considered for this role, we are looking for the following criteria: Essential : NVQ Level 3 in Electrical Installation; 18th Edition of BS7671; Experience of working in domestic properties; Experience in domestic and commercial heating systems; Good understanding and knowledge of Health & Safety in the workplace; Effective communication skills ; Ability to work autonomously as well as part of a successful team; Full UK driving license Desirable : Inspection and Testing Qualification (2391 or 2394/2395) Experience of undertaking Electrical Inspection, Testing and remedial works JIB Gold Card It is a great place to work and this role will provide you with the opportunity to develop your skills and qualifications and as a result, enhance your career. Tools will be provided to successfully perform in your role, such as a company vehicle, full company uniform, tablet and mobile. In return for your commitment they offer an excellent competitive salary and benefits package such as: pension scheme; free platinum boiler cover; discounts from many different retailers, 22 days holiday plus bank holidays ( increasing with length of service ); opportunity to buy and sell holiday; life insurance; life assurance scheme and company sick pay.
PPD's mission is to improve health. It starts as an idea to cure. It becomes a life saved. All in-between, it's you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. PPD's Project Management department is a global team organized by therapeutic area. We partner directly with our clients to deliver projects from study start-up through close-out activities. In Project Management, you will oversee the delivery of PPD groups collaborating to support our clients. In short, you are a crucial piece in earning the trust of our clients. We are seeking a new Senior Project Manager/Associate Director (Delivery) in our Early Phase Development Project Management Team in the EMEA region. This is permanent full time role and can be office or homebased. As a Project Manager, you are responsible for the overall management and successful delivery of the clinical study from start-up through close-out activities. You often work globally, with multi-functional leads to anticipate problems, find solutions and deliver results. You lead the collaboration that shows our clients we are one team focused on our purpose, mission, and strategy. *Responsibilities:* This position is responsible for directing and leading the activities in the Early Phase area within and accountable for the P&L of a specific projects. Develops and drives the specific and overall early phase strategies to ensure optimum performance and achievement of annual plans and targets. Has overall responsibility for instigating and leading change initiatives within the phase one area and works with peers of EDS in the overall leadership of the Project Management group. *Qualifications:* * Education and Experience: * * Bachelor's degree or licensed certified health care training; * Demonstrated track record of success in clinical development (equivalent to 7 years) and in leading and developing professional staff in a project led environment; * In depth understanding and experience with budgeting, forecasting and resource management within the Early Phase area; * Experience using project management software; * Valid Passport, where appropriate; * Or equivalent combination of education and experience that provides the individual with the required knowledge, skills and abilities. * Knowledge, Skills and Abilities: * * Knowledge of the key principles of cross functional project management (Time, Quality, Cost); * Solid financial acumen; * Applies a range of negotiation techniques to achieve desired outcomes with evidence of commercial and organizational acumen; * Displays effective communication skills (listening, oral, written) and can communicate in English language (oral, written); * Sound interpersonal skills, is flexible and adapts to changing situations; * Has the ability to persuade, convince, and influence or impress others; * Is organized, proficient at multi-tasking with good attention to detail; * Able to lead, motivate and coordinate teams. Coach/mentor team members as appropriate; * Able to delegate, effectively prioritizes own and workload of project team members; * Ability to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc.; * Possesses cross cultural awareness and is able to adapt appropriately; * Has an understanding and appreciation of clinical research/development, including medical and therapeutic areas, phases and medical terminology; Has knowledge/understanding of clinical development guidelines and Directives. Has experience with leading, liaising and coordinating cross-functional project teams; At PPD we hire the best, develop ourselves and each other, and recognise the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD you will benefit from an award-winning learning and development programme, ensuring you reach your potential. As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture , where PPD truly value a work-life balance. We've grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel. - We have a strong will to win - We earn our customer's trust - We are gamechangers - We do the right thing -We are one PPD - If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, then please submit your application - we'd love to hear from you. #LI-Remote #LI-MC2
Dec 02, 2020
Full time
PPD's mission is to improve health. It starts as an idea to cure. It becomes a life saved. All in-between, it's you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. PPD's Project Management department is a global team organized by therapeutic area. We partner directly with our clients to deliver projects from study start-up through close-out activities. In Project Management, you will oversee the delivery of PPD groups collaborating to support our clients. In short, you are a crucial piece in earning the trust of our clients. We are seeking a new Senior Project Manager/Associate Director (Delivery) in our Early Phase Development Project Management Team in the EMEA region. This is permanent full time role and can be office or homebased. As a Project Manager, you are responsible for the overall management and successful delivery of the clinical study from start-up through close-out activities. You often work globally, with multi-functional leads to anticipate problems, find solutions and deliver results. You lead the collaboration that shows our clients we are one team focused on our purpose, mission, and strategy. *Responsibilities:* This position is responsible for directing and leading the activities in the Early Phase area within and accountable for the P&L of a specific projects. Develops and drives the specific and overall early phase strategies to ensure optimum performance and achievement of annual plans and targets. Has overall responsibility for instigating and leading change initiatives within the phase one area and works with peers of EDS in the overall leadership of the Project Management group. *Qualifications:* * Education and Experience: * * Bachelor's degree or licensed certified health care training; * Demonstrated track record of success in clinical development (equivalent to 7 years) and in leading and developing professional staff in a project led environment; * In depth understanding and experience with budgeting, forecasting and resource management within the Early Phase area; * Experience using project management software; * Valid Passport, where appropriate; * Or equivalent combination of education and experience that provides the individual with the required knowledge, skills and abilities. * Knowledge, Skills and Abilities: * * Knowledge of the key principles of cross functional project management (Time, Quality, Cost); * Solid financial acumen; * Applies a range of negotiation techniques to achieve desired outcomes with evidence of commercial and organizational acumen; * Displays effective communication skills (listening, oral, written) and can communicate in English language (oral, written); * Sound interpersonal skills, is flexible and adapts to changing situations; * Has the ability to persuade, convince, and influence or impress others; * Is organized, proficient at multi-tasking with good attention to detail; * Able to lead, motivate and coordinate teams. Coach/mentor team members as appropriate; * Able to delegate, effectively prioritizes own and workload of project team members; * Ability to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc.; * Possesses cross cultural awareness and is able to adapt appropriately; * Has an understanding and appreciation of clinical research/development, including medical and therapeutic areas, phases and medical terminology; Has knowledge/understanding of clinical development guidelines and Directives. Has experience with leading, liaising and coordinating cross-functional project teams; At PPD we hire the best, develop ourselves and each other, and recognise the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD you will benefit from an award-winning learning and development programme, ensuring you reach your potential. As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture , where PPD truly value a work-life balance. We've grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel. - We have a strong will to win - We earn our customer's trust - We are gamechangers - We do the right thing -We are one PPD - If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, then please submit your application - we'd love to hear from you. #LI-Remote #LI-MC2
We're looking for a candidate to this position in an exciting company. Provide inspirational leadership to a direct team of 20 associates and a regional matrixed team, attract top talent, and align capabilities with current and future business needs while driving a culture of accountability and ownership in the team. Lead the development of the annual strategic plan for Linx by facilitating the process, seeking input, collating insights and aligning internal stakeholders across geographies and functions. Develop and coordinate ongoing VOC efforts for the organization. Develop and maintain knowledge of the market, direct and emerging competitors, technology trends, and emerging applications. Identify and prioritize market opportunities for the organization. Oversee product strategy and portfolio roadmap development including digital transformation initiative to have a competitive offering in the marketplace. Act with global mindset incorporating varying geographic needs into portfolio strategy and go to market activities. Ensure all product launches follow the Launch Excellence framework and meet launch targets. Build the Linx brand globally to drive awareness and increase Net Promoter Score. Generate revenue through channel and direct digital marketing. Manage marketing budget to ensure expense targets are met and forecasted correctly. Apply Danaher Business System resulting in a lean and efficient commercial organization, and Daily Management/Process Orientation. Minimum of 15 years relevant commercial experience, with a minimum of 5 years marketing experience with industrial products. Demonstrated experience in all stages of product lifecycle from initial opportunity through obsolescence. Clear evidence of developing team members to take on broader assignments and grow their careers. Bachelor's Degree in Marketing, Business, Engineering or a related field required. MBA preferred. Ability and willingness to travel up to 40% of the time.
Dec 02, 2020
Full time
We're looking for a candidate to this position in an exciting company. Provide inspirational leadership to a direct team of 20 associates and a regional matrixed team, attract top talent, and align capabilities with current and future business needs while driving a culture of accountability and ownership in the team. Lead the development of the annual strategic plan for Linx by facilitating the process, seeking input, collating insights and aligning internal stakeholders across geographies and functions. Develop and coordinate ongoing VOC efforts for the organization. Develop and maintain knowledge of the market, direct and emerging competitors, technology trends, and emerging applications. Identify and prioritize market opportunities for the organization. Oversee product strategy and portfolio roadmap development including digital transformation initiative to have a competitive offering in the marketplace. Act with global mindset incorporating varying geographic needs into portfolio strategy and go to market activities. Ensure all product launches follow the Launch Excellence framework and meet launch targets. Build the Linx brand globally to drive awareness and increase Net Promoter Score. Generate revenue through channel and direct digital marketing. Manage marketing budget to ensure expense targets are met and forecasted correctly. Apply Danaher Business System resulting in a lean and efficient commercial organization, and Daily Management/Process Orientation. Minimum of 15 years relevant commercial experience, with a minimum of 5 years marketing experience with industrial products. Demonstrated experience in all stages of product lifecycle from initial opportunity through obsolescence. Clear evidence of developing team members to take on broader assignments and grow their careers. Bachelor's Degree in Marketing, Business, Engineering or a related field required. MBA preferred. Ability and willingness to travel up to 40% of the time.
A great opportunity has arisen with a leading national kitchen retailer and manufacturer for a senior kitchen sales designer or showroom manager to take the next step in their career and become a regional multisite sales manager. Overseeing a few showrooms within the Midlands region this role will focus on people management, supporting the kitchen designers to maximise sales opportunities and makin...... click apply for full job details
Dec 02, 2020
Full time
A great opportunity has arisen with a leading national kitchen retailer and manufacturer for a senior kitchen sales designer or showroom manager to take the next step in their career and become a regional multisite sales manager. Overseeing a few showrooms within the Midlands region this role will focus on people management, supporting the kitchen designers to maximise sales opportunities and makin...... click apply for full job details
Segment Marketing Manager - Packaging Print Systems £65,000 plus 20% Bonus and Benefits Cambridge, South East UK The client is an international corporate, which develops and manufactures cutting-edge technology and consumables within the digital print sector. Their state-of-the-art facilities encompass highly capable R&D resources, and they collaborate and partner with a plethora of international...... click apply for full job details
Dec 02, 2020
Full time
Segment Marketing Manager - Packaging Print Systems £65,000 plus 20% Bonus and Benefits Cambridge, South East UK The client is an international corporate, which develops and manufactures cutting-edge technology and consumables within the digital print sector. Their state-of-the-art facilities encompass highly capable R&D resources, and they collaborate and partner with a plethora of international...... click apply for full job details
PPD's mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it's you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. Our Project Delivery team directs, coordinates and manages the technical and operational aspects of projects, securing the successful completion of clinical trials. We collaborate with functional area leads to identify and evaluate fundamental issues on the project and ensure that solutions are implemented. The *Project Manager/Senior Project Manager - Consumer Health* is responsible for the overall coordination and management of consumer health clinical trials and non-interventional studies from start up through close out activities. Directs the technical and operational aspects of the projects, securing the successful completion of clinical trials At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and well being of our employees. *Summarized Purpose: * * * Responsible for the overall coordination and management of of consumer health clinical trials and non-interventional studies from start up through close out activities. Directs the technical and operational aspects of the projects, securing the successful completion of clinical trials. Works with major functional area leads to identify and evaluate fundamental issues on the project, interpret data on complex issues, makes sound business decisions and ensure solutions are implemented. Works to ensure all project deliverables meet the customer's time/quality/cost expectations. Accountable for ensuring all project deliverables meet the customer/contract expectations, providing accurate hour forecasts, reviewing pass-through costs and ensuring timely invoicing with the support of Project Management Directors and/or Associate Directors while working in collaboration with other functional area leads. May work with Directors and/or Associate Directors, Project Management and Contracts & Proposals Development on the development of new proposals and general capabilities presentations to Customers for new business. *Essential Functions:* * Manages allocated studies according to timelines and quality standards. Coordinates activities of all functional departments and vendors involved in the project. Works with team and management to develop plans/guidelines for project implementation using PPD tools. Monitors and analyzes project status to ensure successful completion of project parameters, milestones, timetables (i.e., regulatory document, research agreement, site payments, interim monitoring, CRF retrieval, CRF data entry, etc.). Ensures teams are entering and updating internal tracking tools e.g. Project Pulse, CASCADE, etc. Works with team to identify potential risks, develop contingency plans * Acts as principal liaison between Sponsor and PPD by facilitating the flow of information between PPD and client. Provides Sponsor with timely project updates, project related fiscal information, ensures correct protocol interpretations, and obtains direction and feedback on implementing scope of work. May discuss and obtain feedback from Sponsors regarding PPD's performance to date * Plans and communicates to team members study specific tasks and priorities for projects. Delegates, as appropriate, assigned responsibilities to project team members. Liaises with managers in all functional areas within PPD to optimize performance and utilization of the project team members. Appropriately escalates any issues or potential issues to the Project Management Director or Associate Director for all project related issues * Works closely with finance and legal to manage all financial and contractual aspects of the study including establishing and recognizing financial milestones for invoice and subcontractor purposes, subcontracting with third-party service providers, approving subcontractor invoices, establishing proper accrual for investigator grants, assisting with negotiation of the investigator grants as needed and similar pass-throughs * Works with the project team to establish appropriate controls to ensure that project resources and expenses are aligned with budgets. Works closely with Project Management Director or Associate Director to provide details for the development and negotiation of contract modifications, as needed. Ensures that appropriate assessment and coordination of project/protocol specific and therapeutic area training needs and activities are occurring for the team members as needed * Provides input into hiring, performance management, training and other activities related to leading project staff members across functional areas. * Works to prepare and present at client meetings as the assigned Project Manager. Attends bid defenses as necessary. *Qualifications:* *Education and Experience: * Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years' for Sr PM level) or equivalent combination of education, training, & experience. Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions. *Knowledge, Skills and Abilities: * * Knowledge of the key principles of cross functional project management (Time, Quality, Cost). * Solid financial acumen. * Applies a range of negotiation techniques to achieve desired outcomes with evidence of commercial and organizational acumen. * Can effectively plan and deliver a dynamic and persuasive presentation, using effective graphics, overheads or slides. * Displays effective communication skills (listening, oral, written) and can communicate in English language (oral, written). * Sound interpersonal skills, is flexible and adapts to changing situations. * Has the ability to persuade, convince, and influence or impress others. * Is organized, proficient at multi-tasking with good attention to detail * Able to lead, motivate and coordinate teams. Coach/mentor team members as appropriate. * Able to delegate, effectively prioritizes own and workload of project team members. * Ability to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc. * Possesses cross cultural awareness and is able to adapt appropriately. * Has an in-depth understanding and appreciation of clinical research/development, including medical and therapeutic areas, phases and medical terminology. * Has experience with leading, liaising and coordinating cross-functional project teams. * Has an in-depth knowledge/understanding of clinical development guidelines and directives *PPD Defining Principles: * - We have a strong will to win - We earn our customer's trust - We are game changers - We do the right thing - We are one PPD - If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, then please submit your application - we'd love to hear from you.
Dec 02, 2020
Full time
PPD's mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it's you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. Our Project Delivery team directs, coordinates and manages the technical and operational aspects of projects, securing the successful completion of clinical trials. We collaborate with functional area leads to identify and evaluate fundamental issues on the project and ensure that solutions are implemented. The *Project Manager/Senior Project Manager - Consumer Health* is responsible for the overall coordination and management of consumer health clinical trials and non-interventional studies from start up through close out activities. Directs the technical and operational aspects of the projects, securing the successful completion of clinical trials At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and well being of our employees. *Summarized Purpose: * * * Responsible for the overall coordination and management of of consumer health clinical trials and non-interventional studies from start up through close out activities. Directs the technical and operational aspects of the projects, securing the successful completion of clinical trials. Works with major functional area leads to identify and evaluate fundamental issues on the project, interpret data on complex issues, makes sound business decisions and ensure solutions are implemented. Works to ensure all project deliverables meet the customer's time/quality/cost expectations. Accountable for ensuring all project deliverables meet the customer/contract expectations, providing accurate hour forecasts, reviewing pass-through costs and ensuring timely invoicing with the support of Project Management Directors and/or Associate Directors while working in collaboration with other functional area leads. May work with Directors and/or Associate Directors, Project Management and Contracts & Proposals Development on the development of new proposals and general capabilities presentations to Customers for new business. *Essential Functions:* * Manages allocated studies according to timelines and quality standards. Coordinates activities of all functional departments and vendors involved in the project. Works with team and management to develop plans/guidelines for project implementation using PPD tools. Monitors and analyzes project status to ensure successful completion of project parameters, milestones, timetables (i.e., regulatory document, research agreement, site payments, interim monitoring, CRF retrieval, CRF data entry, etc.). Ensures teams are entering and updating internal tracking tools e.g. Project Pulse, CASCADE, etc. Works with team to identify potential risks, develop contingency plans * Acts as principal liaison between Sponsor and PPD by facilitating the flow of information between PPD and client. Provides Sponsor with timely project updates, project related fiscal information, ensures correct protocol interpretations, and obtains direction and feedback on implementing scope of work. May discuss and obtain feedback from Sponsors regarding PPD's performance to date * Plans and communicates to team members study specific tasks and priorities for projects. Delegates, as appropriate, assigned responsibilities to project team members. Liaises with managers in all functional areas within PPD to optimize performance and utilization of the project team members. Appropriately escalates any issues or potential issues to the Project Management Director or Associate Director for all project related issues * Works closely with finance and legal to manage all financial and contractual aspects of the study including establishing and recognizing financial milestones for invoice and subcontractor purposes, subcontracting with third-party service providers, approving subcontractor invoices, establishing proper accrual for investigator grants, assisting with negotiation of the investigator grants as needed and similar pass-throughs * Works with the project team to establish appropriate controls to ensure that project resources and expenses are aligned with budgets. Works closely with Project Management Director or Associate Director to provide details for the development and negotiation of contract modifications, as needed. Ensures that appropriate assessment and coordination of project/protocol specific and therapeutic area training needs and activities are occurring for the team members as needed * Provides input into hiring, performance management, training and other activities related to leading project staff members across functional areas. * Works to prepare and present at client meetings as the assigned Project Manager. Attends bid defenses as necessary. *Qualifications:* *Education and Experience: * Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years' for Sr PM level) or equivalent combination of education, training, & experience. Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions. *Knowledge, Skills and Abilities: * * Knowledge of the key principles of cross functional project management (Time, Quality, Cost). * Solid financial acumen. * Applies a range of negotiation techniques to achieve desired outcomes with evidence of commercial and organizational acumen. * Can effectively plan and deliver a dynamic and persuasive presentation, using effective graphics, overheads or slides. * Displays effective communication skills (listening, oral, written) and can communicate in English language (oral, written). * Sound interpersonal skills, is flexible and adapts to changing situations. * Has the ability to persuade, convince, and influence or impress others. * Is organized, proficient at multi-tasking with good attention to detail * Able to lead, motivate and coordinate teams. Coach/mentor team members as appropriate. * Able to delegate, effectively prioritizes own and workload of project team members. * Ability to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc. * Possesses cross cultural awareness and is able to adapt appropriately. * Has an in-depth understanding and appreciation of clinical research/development, including medical and therapeutic areas, phases and medical terminology. * Has experience with leading, liaising and coordinating cross-functional project teams. * Has an in-depth knowledge/understanding of clinical development guidelines and directives *PPD Defining Principles: * - We have a strong will to win - We earn our customer's trust - We are game changers - We do the right thing - We are one PPD - If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, then please submit your application - we'd love to hear from you.
Oncology Hospital Sales Representative, East of England covering Norfolk, Suffolk, Cambridge and Essex Specialist Hospital Sales Representative within the Oncology Business Unit, the successful candidate will be required to implement projects and initiatives across a range of accounts and work collaboratively with their Healthcare Development Manager (HDM). Key role remit: To successfully and effectively sell key brands to key clinicians and stakeholders within the patient pathway to ensure our commercial success within the region and their territory. To work with the Regional leadership team (RLT) to identify key customers who may be used throughout the region as speakers at promotional meetings To develop & manage relationships with key customers within priority accounts as established with the RLT To effectively and efficiently manage your time to ensure we achieve key territory and brand objectives within the POA Work with your RLT to write best in class business plans for priority accounts Develop a target customer list which will allow the maximum ROI for the territory Confidently challenge the RLT when new information has been identified based upon key customer insights which will allow plans to be updated or amended Detailed sales analysis required to comprehend the performance of key accounts and be able to demonstrate how these insights are driving your activity and focus Appropriately manage OBU resources; Deliver established activity metrics in line with territory and district business plans Appropriately manage territory budget and ensure that any over or under spend is highlighted in a timely manner to the RLT to allow resource reallocation.
Dec 02, 2020
Full time
Oncology Hospital Sales Representative, East of England covering Norfolk, Suffolk, Cambridge and Essex Specialist Hospital Sales Representative within the Oncology Business Unit, the successful candidate will be required to implement projects and initiatives across a range of accounts and work collaboratively with their Healthcare Development Manager (HDM). Key role remit: To successfully and effectively sell key brands to key clinicians and stakeholders within the patient pathway to ensure our commercial success within the region and their territory. To work with the Regional leadership team (RLT) to identify key customers who may be used throughout the region as speakers at promotional meetings To develop & manage relationships with key customers within priority accounts as established with the RLT To effectively and efficiently manage your time to ensure we achieve key territory and brand objectives within the POA Work with your RLT to write best in class business plans for priority accounts Develop a target customer list which will allow the maximum ROI for the territory Confidently challenge the RLT when new information has been identified based upon key customer insights which will allow plans to be updated or amended Detailed sales analysis required to comprehend the performance of key accounts and be able to demonstrate how these insights are driving your activity and focus Appropriately manage OBU resources; Deliver established activity metrics in line with territory and district business plans Appropriately manage territory budget and ensure that any over or under spend is highlighted in a timely manner to the RLT to allow resource reallocation.
Group Leader: Target Validation and Disease Positioning Location: The Francis Crick Institute, London Contract: Permanent, 35 hours per week. (flexible working requests will be considered) Closing date: Midnight 6th December 2020. Please do not delay applying, we will be shortlisting and interviewing on application. Salary: £52,00 - £62,000 (may have some flexibility for the right candidate) Application process: CV and application questions via our careers page. Do you want to help deliver breakthrough medicines for cancer patients? Cancer Research UK's Therapeutic Discovery Laboratories (CRUK-TDL) is the in-house CRUK drug discovery unit with a principal focus on establishing and prosecuting biologically-themed multi-project alliances with industrial partners. Based at the Francis Crick Insitute and the Babraham Research Campus, Cambridge, TDL comprises over 90 staff from both industrial and academic backgrounds. There is now an exciting opportunity available for a talented and ambitious drug discovery scientist to join the Therapeutic Discovery Laboratories in Cambridge as a Group Leader in the Target Validation and Disease Positioning (TVDP) team. The TVDP team is comprised of highly skilled cancer cell biologists and immunologists working across the entire drug discovery pipeline and alliance portfolio. Expertise spans target sourcing and validation, clinical positioning and bioinformatics, and the team routinely performs genetic manipulation, proof of concept and mechanism of action studies and novel cellular assay development. What will you be doing? Leading, mentoring and developing a team of 5-10 cell biologists. Responsible for setting and maintaining the highest scientific standards Providing flexible project support and motivating team members to maximise their potential. Developing of future TVDP capability and expertise Critical input into target and alliance prosecution rationale Oversight of a themed area of biology and/or lead one or more projects and play a leading role in interactions with our academic and industry partners. You can find out more about the role and TDL in our candidate pack Who we're looking for: Innovative scientist with a strong background in oncology and a track record of delivery in drug discovery Strong leadership skills with a passion for developing others External network and scientific presence with the ability to forge relationships, and work in collaboration, with both academic and industrial stake-holders Experience of driving operational and scientific innovations Flexible mindset, with the ability to adapt to new challenges If this sounds like a challenge you have the motivation and experience to take on, we would love to hear from you. What will I gain? You'll be making a real difference to people's lives - we're the largest global Cancer Research charity. There's plenty of career progression and training opportunities, through internal and external L&D. 25, days annual leave (plus bank holidays and the ability to buy up to 5 days per annum) and 1 CRUK day. Pension (employer contributions of up to 10%), life insurance and a great benefit discount platform. If you're as ambitious as we are, join our collective force and enjoy an excellent career, as we save lives and add years.
Dec 02, 2020
Full time
Group Leader: Target Validation and Disease Positioning Location: The Francis Crick Institute, London Contract: Permanent, 35 hours per week. (flexible working requests will be considered) Closing date: Midnight 6th December 2020. Please do not delay applying, we will be shortlisting and interviewing on application. Salary: £52,00 - £62,000 (may have some flexibility for the right candidate) Application process: CV and application questions via our careers page. Do you want to help deliver breakthrough medicines for cancer patients? Cancer Research UK's Therapeutic Discovery Laboratories (CRUK-TDL) is the in-house CRUK drug discovery unit with a principal focus on establishing and prosecuting biologically-themed multi-project alliances with industrial partners. Based at the Francis Crick Insitute and the Babraham Research Campus, Cambridge, TDL comprises over 90 staff from both industrial and academic backgrounds. There is now an exciting opportunity available for a talented and ambitious drug discovery scientist to join the Therapeutic Discovery Laboratories in Cambridge as a Group Leader in the Target Validation and Disease Positioning (TVDP) team. The TVDP team is comprised of highly skilled cancer cell biologists and immunologists working across the entire drug discovery pipeline and alliance portfolio. Expertise spans target sourcing and validation, clinical positioning and bioinformatics, and the team routinely performs genetic manipulation, proof of concept and mechanism of action studies and novel cellular assay development. What will you be doing? Leading, mentoring and developing a team of 5-10 cell biologists. Responsible for setting and maintaining the highest scientific standards Providing flexible project support and motivating team members to maximise their potential. Developing of future TVDP capability and expertise Critical input into target and alliance prosecution rationale Oversight of a themed area of biology and/or lead one or more projects and play a leading role in interactions with our academic and industry partners. You can find out more about the role and TDL in our candidate pack Who we're looking for: Innovative scientist with a strong background in oncology and a track record of delivery in drug discovery Strong leadership skills with a passion for developing others External network and scientific presence with the ability to forge relationships, and work in collaboration, with both academic and industrial stake-holders Experience of driving operational and scientific innovations Flexible mindset, with the ability to adapt to new challenges If this sounds like a challenge you have the motivation and experience to take on, we would love to hear from you. What will I gain? You'll be making a real difference to people's lives - we're the largest global Cancer Research charity. There's plenty of career progression and training opportunities, through internal and external L&D. 25, days annual leave (plus bank holidays and the ability to buy up to 5 days per annum) and 1 CRUK day. Pension (employer contributions of up to 10%), life insurance and a great benefit discount platform. If you're as ambitious as we are, join our collective force and enjoy an excellent career, as we save lives and add years.
Office For National Statistics
Cambridge, Cambridgeshire
Communal establishments officers 25 hours a week Contract: 16 February 2021 to 14 April 2021 plus holiday Salary dependent on location Band 1 - £14.61 Band 2 - £12.64 Band 3 - £11.22 No fixed daily working hours but you must work within the following times: Monday to Saturday: 9am and 8pm Sundays and bank holidays: 10am and 4pm Confident communicators make the census The census is a survey of the entire population of England and Wales that happens every 10 years. It's run by the Office for National Statistics (ONS) and gives us a picture of all the people and households in England and Wales. The information we collect is used to make decisions that affect everyone - things like how many schools, surgeries and hospitals we need. To help us, we need a field team to encourage people in communal establishments (CEs) to take part. CEs are managed residential accommodations such as universities and care homes, so you will meet people from all walks of life. The role In this flexible, temporary role, you will make contact with and visit addresses of CEs, to either deliver or follow up on census questionnaires. Most of your work will be face-to-face, but you will need to make phone calls ahead of some visits, building relationships with accommodation managers and residents to encourage them to take part. You will also help people overcome any objections or barriers to completing the questionnaire either by assisting them yourself or referring them to available support. You will work in a team with assistance and guidance from your team leader, who will meet with you when you are working to help you settle into your role. Your hours will be flexible to help you maximise engagement with the CE populations you need to reach. About you You are an outgoing, confident communicator and you are at ease using smartphones and tablets. You likely have previous customer service experience, and you will be comfortable speaking to members of the public in their own homes. A team player, you are professional and calm in challenging situations. You will be out and about visiting addresses, so you must be prepared to travel. You will need a current, full UK driving license and use of a motor vehicle, insured for business use. We will pay travel expenses within your work area. For roles in Wales, knowledge of Welsh would be an advantage. To be considered for the role, you must be available from 16 February 2020 to 14 April 2021 inclusive. You will also need to be flexible with your hours, because you might have to work evenings and weekends, depending on the accommodation you are visiting. People make the census. If you are comfortable interacting with the public and interested in making Census 2021 a success for everyone, apply for a communal establishments officer role. We can only employ you if you are eligible to work for the Civil Service. Find out more about the Civil Service nationality rules . COVID-19 Your health, and that of our field staff, is very important to us. We will be following the government's safety guidelines about the coronavirus (COVID-19). Appropriate PPE (Personal Protective Equipment) will be provided to all staff. Social distancing will be maintained throughout the operation.
Dec 02, 2020
Full time
Communal establishments officers 25 hours a week Contract: 16 February 2021 to 14 April 2021 plus holiday Salary dependent on location Band 1 - £14.61 Band 2 - £12.64 Band 3 - £11.22 No fixed daily working hours but you must work within the following times: Monday to Saturday: 9am and 8pm Sundays and bank holidays: 10am and 4pm Confident communicators make the census The census is a survey of the entire population of England and Wales that happens every 10 years. It's run by the Office for National Statistics (ONS) and gives us a picture of all the people and households in England and Wales. The information we collect is used to make decisions that affect everyone - things like how many schools, surgeries and hospitals we need. To help us, we need a field team to encourage people in communal establishments (CEs) to take part. CEs are managed residential accommodations such as universities and care homes, so you will meet people from all walks of life. The role In this flexible, temporary role, you will make contact with and visit addresses of CEs, to either deliver or follow up on census questionnaires. Most of your work will be face-to-face, but you will need to make phone calls ahead of some visits, building relationships with accommodation managers and residents to encourage them to take part. You will also help people overcome any objections or barriers to completing the questionnaire either by assisting them yourself or referring them to available support. You will work in a team with assistance and guidance from your team leader, who will meet with you when you are working to help you settle into your role. Your hours will be flexible to help you maximise engagement with the CE populations you need to reach. About you You are an outgoing, confident communicator and you are at ease using smartphones and tablets. You likely have previous customer service experience, and you will be comfortable speaking to members of the public in their own homes. A team player, you are professional and calm in challenging situations. You will be out and about visiting addresses, so you must be prepared to travel. You will need a current, full UK driving license and use of a motor vehicle, insured for business use. We will pay travel expenses within your work area. For roles in Wales, knowledge of Welsh would be an advantage. To be considered for the role, you must be available from 16 February 2020 to 14 April 2021 inclusive. You will also need to be flexible with your hours, because you might have to work evenings and weekends, depending on the accommodation you are visiting. People make the census. If you are comfortable interacting with the public and interested in making Census 2021 a success for everyone, apply for a communal establishments officer role. We can only employ you if you are eligible to work for the Civil Service. Find out more about the Civil Service nationality rules . COVID-19 Your health, and that of our field staff, is very important to us. We will be following the government's safety guidelines about the coronavirus (COVID-19). Appropriate PPE (Personal Protective Equipment) will be provided to all staff. Social distancing will be maintained throughout the operation.
Earn while you train Why not consider training as a Hearing Aid Dispenser with Hidden Hearing? Hidden Hearing is one of the largest providers of independent hearing care in the UK. We have over 80 branches, 120 qualified Hearing Aid Dispensers and conduct over 100,000 hearing assessments each year...... click apply for full job details
Dec 02, 2020
Full time
Earn while you train Why not consider training as a Hearing Aid Dispenser with Hidden Hearing? Hidden Hearing is one of the largest providers of independent hearing care in the UK. We have over 80 branches, 120 qualified Hearing Aid Dispensers and conduct over 100,000 hearing assessments each year...... click apply for full job details
#16529| 12 months+ | Cambridge James Carrera at Umbilical has partnered with an established Pharmaceutical client to source a Regulatory Affairs Associate to join and support an established International Regulatory Team. Accountable for: Supports regulatory teams by providing a proof reading and Quality Assurance (QA) check resource for regulatory product information annexes...... click apply for full job details
Dec 02, 2020
Contractor
#16529| 12 months+ | Cambridge James Carrera at Umbilical has partnered with an established Pharmaceutical client to source a Regulatory Affairs Associate to join and support an established International Regulatory Team. Accountable for: Supports regulatory teams by providing a proof reading and Quality Assurance (QA) check resource for regulatory product information annexes...... click apply for full job details
Oncology Hospital Sales Representative, East of England covering Norfolk, Suffolk, Cambridge and Essex Specialist Hospital Sales Representative within the Oncology Business Unit, the successful candidate will be required to implement projects and initiatives across a range of accounts and work collaboratively with their Healthcare Development Manager (HDM). Key role remit: To successfully and effectively sell key brands to key clinicians and stakeholders within the patient pathway to ensure our commercial success within the region and their territory. To work with the Regional leadership team (RLT) to identify key customers who may be used throughout the region as speakers at promotional meetings To develop & manage relationships with key customers within priority accounts as established with the RLT To effectively and efficiently manage your time to ensure we achieve key territory and brand objectives within the POA Work with your RLT to write best in class business plans for priority accounts Develop a target customer list which will allow the maximum ROI for the territory Confidently challenge the RLT when new information has been identified based upon key customer insights which will allow plans to be updated or amended Detailed sales analysis required to comprehend the performance of key accounts and be able to demonstrate how these insights are driving your activity and focus Appropriately manage OBU resources; Deliver established activity metrics in line with territory and district business plans Appropriately manage territory budget and ensure that any over or under spend is highlighted in a timely manner to the RLT to allow resource reallocation.
Dec 02, 2020
Full time
Oncology Hospital Sales Representative, East of England covering Norfolk, Suffolk, Cambridge and Essex Specialist Hospital Sales Representative within the Oncology Business Unit, the successful candidate will be required to implement projects and initiatives across a range of accounts and work collaboratively with their Healthcare Development Manager (HDM). Key role remit: To successfully and effectively sell key brands to key clinicians and stakeholders within the patient pathway to ensure our commercial success within the region and their territory. To work with the Regional leadership team (RLT) to identify key customers who may be used throughout the region as speakers at promotional meetings To develop & manage relationships with key customers within priority accounts as established with the RLT To effectively and efficiently manage your time to ensure we achieve key territory and brand objectives within the POA Work with your RLT to write best in class business plans for priority accounts Develop a target customer list which will allow the maximum ROI for the territory Confidently challenge the RLT when new information has been identified based upon key customer insights which will allow plans to be updated or amended Detailed sales analysis required to comprehend the performance of key accounts and be able to demonstrate how these insights are driving your activity and focus Appropriately manage OBU resources; Deliver established activity metrics in line with territory and district business plans Appropriately manage territory budget and ensure that any over or under spend is highlighted in a timely manner to the RLT to allow resource reallocation.
*Senior or Principal Statistical Programmer - Late R&I* *Location: Cambridge, UK* *Competitive financial package* Are you a *Statistical Programmer* eager to apply your knowledge and skills in a truly meaningful setting? Would you like to play a key role the development of medicines to patients? If so, we would love to hear from you! At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person. Our Late R&I Biometrics team is dedicated to the development of innovative treatment of Respiratory and Immunology (R&I) diseases. You will join a global, diverse and cross-functional environment where you will get personal and professional development. Welcome to Cambridge (UK), one of over 400 sites here at AstraZeneca, providing a collaborative environment where everyone feels comfortable and able to be themselves is at the core of AstraZeneca's priorities, it's important to us that you bring your full self to work every day. In this role, we will give you the chance to utilise your statistical programming expertise in analysis and reporting of clinical trial programs; submission and defence of regulatory filings and the generation of evidence to support product commercialisation and reimbursement. *Main Duties and Responsibilities* Depending on your previous experience and education, you will use and develop your programmer know-how in a data driven environment. You may already be equipped to lead programmer employees, either by technical leadership or line management. We offer a role suited for your competence. Your responsibilities will include: * Statistical programming deliverables for regulatory submissions, including specification and delivery of coordinated databases, outputs and response to regulatory questions; commercialisation and reimbursements * Delivery of the Clinical Study Report (CSR), Study Data Tabulation Model (SDTM)/Analysis Data Model (ADaM) databases and Tables, Figures and Listings (TFL) outputs through both internal and external delivery models, following applicable data standards and regulations * Statistical programming contribution to Development Safety Update Reports (DSUR), Periodic Benefit-Risk Evaluation Report (PBRER), Investigators brochures (IB) * Contribute to or lead the statistical programming thinking, analysis and reporting to relevant groups in product and study teams * Development of standard methodology to improve quality, efficiency and effectiveness *Essential Requirements * You are focused on solving challenging problems through collaboration and partnerships. You are a specialist in your field, or aspire to be a specialist, and you know that the best results are achieved by utilising the strengths of every individual. * You have a degree in Mathematics, Computer Science, Statistics, Life Sciences or similar area * You have advanced SAS Programming and CDISC standards knowledge * You possess excellent interpersonal skills * You have experience working in the Respiratory or Vaccine therapeutic area We would like to know more about you. If you are interested, apply now! At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we're opening new ways to work, pioneering cutting edge methods and bringing unexpected teams together. Interested? Come and join our journey. *Deadline for applications is 31st December 2020*
Dec 02, 2020
Full time
*Senior or Principal Statistical Programmer - Late R&I* *Location: Cambridge, UK* *Competitive financial package* Are you a *Statistical Programmer* eager to apply your knowledge and skills in a truly meaningful setting? Would you like to play a key role the development of medicines to patients? If so, we would love to hear from you! At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person. Our Late R&I Biometrics team is dedicated to the development of innovative treatment of Respiratory and Immunology (R&I) diseases. You will join a global, diverse and cross-functional environment where you will get personal and professional development. Welcome to Cambridge (UK), one of over 400 sites here at AstraZeneca, providing a collaborative environment where everyone feels comfortable and able to be themselves is at the core of AstraZeneca's priorities, it's important to us that you bring your full self to work every day. In this role, we will give you the chance to utilise your statistical programming expertise in analysis and reporting of clinical trial programs; submission and defence of regulatory filings and the generation of evidence to support product commercialisation and reimbursement. *Main Duties and Responsibilities* Depending on your previous experience and education, you will use and develop your programmer know-how in a data driven environment. You may already be equipped to lead programmer employees, either by technical leadership or line management. We offer a role suited for your competence. Your responsibilities will include: * Statistical programming deliverables for regulatory submissions, including specification and delivery of coordinated databases, outputs and response to regulatory questions; commercialisation and reimbursements * Delivery of the Clinical Study Report (CSR), Study Data Tabulation Model (SDTM)/Analysis Data Model (ADaM) databases and Tables, Figures and Listings (TFL) outputs through both internal and external delivery models, following applicable data standards and regulations * Statistical programming contribution to Development Safety Update Reports (DSUR), Periodic Benefit-Risk Evaluation Report (PBRER), Investigators brochures (IB) * Contribute to or lead the statistical programming thinking, analysis and reporting to relevant groups in product and study teams * Development of standard methodology to improve quality, efficiency and effectiveness *Essential Requirements * You are focused on solving challenging problems through collaboration and partnerships. You are a specialist in your field, or aspire to be a specialist, and you know that the best results are achieved by utilising the strengths of every individual. * You have a degree in Mathematics, Computer Science, Statistics, Life Sciences or similar area * You have advanced SAS Programming and CDISC standards knowledge * You possess excellent interpersonal skills * You have experience working in the Respiratory or Vaccine therapeutic area We would like to know more about you. If you are interested, apply now! At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we're opening new ways to work, pioneering cutting edge methods and bringing unexpected teams together. Interested? Come and join our journey. *Deadline for applications is 31st December 2020*
Cancer Research UK-AstraZeneca Antibody Alliance Laboratory: Associate Scientist - Protein Sciences Location : Granta Park, Cambridge Contract : Permanent, Full Time (35 hours per week) Salary: £26,000 - £28,000 Closing date: Midnight 15th December 2020. Please do not delay applying as we will be shortlisting on application and may closing date early if we are inundated with applications. Application process: CV and application questions via our careers page You can find out more about the role and AstraZeneca Antibody Alliance Laboratory in our candidate pack Are you a passionate research scientist with a background in Protein Science related discipline looking to develop skills in drug discovery? In collaboration with AstraZeneca, Cancer Research UK (CRUK) has established a pioneering laboratory in Cambridge. The lab deploys cutting edge technologies in order to generate candidate therapeutics, diagnostics and reagent tools. This exciting venture takes AstraZeneca's leading discovery technologies and combine them with biological targets arising from CRUK's extensive network of academic investigators. Why we need you? We are now seeking a research scientist with experience of drug discovery to play a pivotal role in the protein science function of the Alliance Laboratory. The post holder will be part of a multi-disciplinary research team focussed on identifying and characterising biotherapeutic candidates to oncology targets and driving onward development to preclinical proof of concept. What will I be doing? Generating antibody and antibody fragment (scFv and Fab) reagents for the laboratory using mammalian and bacterial expression systems. Maintaining mammalian cell line cultures. Maintain inventory systems to track protein stock levels. Using an AKTA and other automated purification platforms. As well as other analytical techniques such as SDS-PAGE, HPLC and Western blotting. Undertaking molecular biology tasks such as restriction digest cloning. Undertaking the careful QC analysis of targets and antibody reagents for Drug Discovery Building excellent working relationships within a laboratory What skills do I need? Knowledge of how to express and purify proteins Experience with aseptic technique for culturing of cell lines. Knowledge of protein manufacture and associated data logging would be highly beneficial. Excellent communication skills and the ability to communicate across scientific disciplines. What will I gain? Without you we wouldn't be able to achieve our aim of seeing 3 in 4 people survive cancer by 2034. So, we want to reward you in as many ways as possible. There's plenty of career progression and training opportunities, through internal and external L&D. 25, days annual leave (plus bank holidays and the ability to buy up to 5 days per annum) and 1 CRUK day. Pension (employer contributions of up to 10%), life insurance and a great benefit discount platform. If you're as ambitious and passionate as we are, join our collective force and enjoy an excellent career, as we save lives and add years.
Dec 02, 2020
Full time
Cancer Research UK-AstraZeneca Antibody Alliance Laboratory: Associate Scientist - Protein Sciences Location : Granta Park, Cambridge Contract : Permanent, Full Time (35 hours per week) Salary: £26,000 - £28,000 Closing date: Midnight 15th December 2020. Please do not delay applying as we will be shortlisting on application and may closing date early if we are inundated with applications. Application process: CV and application questions via our careers page You can find out more about the role and AstraZeneca Antibody Alliance Laboratory in our candidate pack Are you a passionate research scientist with a background in Protein Science related discipline looking to develop skills in drug discovery? In collaboration with AstraZeneca, Cancer Research UK (CRUK) has established a pioneering laboratory in Cambridge. The lab deploys cutting edge technologies in order to generate candidate therapeutics, diagnostics and reagent tools. This exciting venture takes AstraZeneca's leading discovery technologies and combine them with biological targets arising from CRUK's extensive network of academic investigators. Why we need you? We are now seeking a research scientist with experience of drug discovery to play a pivotal role in the protein science function of the Alliance Laboratory. The post holder will be part of a multi-disciplinary research team focussed on identifying and characterising biotherapeutic candidates to oncology targets and driving onward development to preclinical proof of concept. What will I be doing? Generating antibody and antibody fragment (scFv and Fab) reagents for the laboratory using mammalian and bacterial expression systems. Maintaining mammalian cell line cultures. Maintain inventory systems to track protein stock levels. Using an AKTA and other automated purification platforms. As well as other analytical techniques such as SDS-PAGE, HPLC and Western blotting. Undertaking molecular biology tasks such as restriction digest cloning. Undertaking the careful QC analysis of targets and antibody reagents for Drug Discovery Building excellent working relationships within a laboratory What skills do I need? Knowledge of how to express and purify proteins Experience with aseptic technique for culturing of cell lines. Knowledge of protein manufacture and associated data logging would be highly beneficial. Excellent communication skills and the ability to communicate across scientific disciplines. What will I gain? Without you we wouldn't be able to achieve our aim of seeing 3 in 4 people survive cancer by 2034. So, we want to reward you in as many ways as possible. There's plenty of career progression and training opportunities, through internal and external L&D. 25, days annual leave (plus bank holidays and the ability to buy up to 5 days per annum) and 1 CRUK day. Pension (employer contributions of up to 10%), life insurance and a great benefit discount platform. If you're as ambitious and passionate as we are, join our collective force and enjoy an excellent career, as we save lives and add years.
Cancer Research UK-AstraZeneca Antibody Alliance Laboratory: Associate Scientist Oncology Cell Biology Location : Granta Park, Cambridge Contract : Fixed Term Contract - 12 months, Full Time (35 hours per week) Salary: £26,000 - £29,000 Closing date: Midnight 15th December 2020. Please do not delay applying as we will be shortlisting on application. Application process: CV and application questions via our careers page You can find out more about the role and AstraZeneca Antibody Alliance Laboratory in our candidate pack Are you a passionate research scientist with a background in Oncology Cell Biology looking to develop skills in drug discovery? In collaboration with AstraZeneca, Cancer Research UK (CRUK) has established a pioneering laboratory in Cambridge. The lab deploys cutting edge technologies in order to generate candidate therapeutics, diagnostics and reagent tools. This exciting venture takes AstraZeneca's leading discovery technologies and combine them with biological targets arising from CRUK's extensive network of academic investigators. Why we need you? We are now seeking a research scientist with experience of Oncology cell based assays to play an important role in the Oncology cell based assay group of the Alliance Laboratory. The post holder will be part of a multi-disciplinary research team focussed on identifying and characterising biotherapeutic candidates to oncology targets and driving onward development to preclinical proof of concept. What will I be doing? Maintaining mammalian cell line cultures Running screening assays to characterise antibodies as part the drug discovery cascade Performing cell based experiments to validate and better understand biology of drug targets. Characterising cell lines Generating cell lines Building excellent working relationships within a laboratory What skills do I need? Experience with aspectic technique to enable routine growth of mammalian cell lines is essential. Experience running cell based assays within the context of drug is desirable - ideally with antibodies, but experience of small molecules will be considered beneficial. Familiarity with cell based technologies such as Flow Cytometry would be beneficial. Knowledge of recombinant protein assays including ELISA and HTRF is desirable. Ability to clearly communicate scientific objectives and project results What will I gain? Without you we wouldn't be able to achieve our aim of seeing 3 in 4 people survive cancer by 2034. So, we want to reward you in as many ways as possible. There's plenty of career progression and training opportunities, through internal and external L&D. 25, days annual leave (plus bank holidays and the ability to buy up to 5 days per annum) and 1 CRUK day. Pension (employer contributions of up to 10%), life insurance and a great benefit discount platform. If you're as ambitious and passionate as we are, join our collective force and enjoy an excellent career, as we save lives and add years.
Dec 02, 2020
Full time
Cancer Research UK-AstraZeneca Antibody Alliance Laboratory: Associate Scientist Oncology Cell Biology Location : Granta Park, Cambridge Contract : Fixed Term Contract - 12 months, Full Time (35 hours per week) Salary: £26,000 - £29,000 Closing date: Midnight 15th December 2020. Please do not delay applying as we will be shortlisting on application. Application process: CV and application questions via our careers page You can find out more about the role and AstraZeneca Antibody Alliance Laboratory in our candidate pack Are you a passionate research scientist with a background in Oncology Cell Biology looking to develop skills in drug discovery? In collaboration with AstraZeneca, Cancer Research UK (CRUK) has established a pioneering laboratory in Cambridge. The lab deploys cutting edge technologies in order to generate candidate therapeutics, diagnostics and reagent tools. This exciting venture takes AstraZeneca's leading discovery technologies and combine them with biological targets arising from CRUK's extensive network of academic investigators. Why we need you? We are now seeking a research scientist with experience of Oncology cell based assays to play an important role in the Oncology cell based assay group of the Alliance Laboratory. The post holder will be part of a multi-disciplinary research team focussed on identifying and characterising biotherapeutic candidates to oncology targets and driving onward development to preclinical proof of concept. What will I be doing? Maintaining mammalian cell line cultures Running screening assays to characterise antibodies as part the drug discovery cascade Performing cell based experiments to validate and better understand biology of drug targets. Characterising cell lines Generating cell lines Building excellent working relationships within a laboratory What skills do I need? Experience with aspectic technique to enable routine growth of mammalian cell lines is essential. Experience running cell based assays within the context of drug is desirable - ideally with antibodies, but experience of small molecules will be considered beneficial. Familiarity with cell based technologies such as Flow Cytometry would be beneficial. Knowledge of recombinant protein assays including ELISA and HTRF is desirable. Ability to clearly communicate scientific objectives and project results What will I gain? Without you we wouldn't be able to achieve our aim of seeing 3 in 4 people survive cancer by 2034. So, we want to reward you in as many ways as possible. There's plenty of career progression and training opportunities, through internal and external L&D. 25, days annual leave (plus bank holidays and the ability to buy up to 5 days per annum) and 1 CRUK day. Pension (employer contributions of up to 10%), life insurance and a great benefit discount platform. If you're as ambitious and passionate as we are, join our collective force and enjoy an excellent career, as we save lives and add years.
Facilities Support Technician Are you a natural problem solver and fixer? Do you have outstanding customer service skills? We have a challenging and exciting role for Facilities Support Technician to join us on a 12 month fixed term basis working alongside our Facilities Manager and Support Technician. You will be expected to promote and manage the facilities helpdesk, assist with regulatory site in...... click apply for full job details
Dec 02, 2020
Contractor
Facilities Support Technician Are you a natural problem solver and fixer? Do you have outstanding customer service skills? We have a challenging and exciting role for Facilities Support Technician to join us on a 12 month fixed term basis working alongside our Facilities Manager and Support Technician. You will be expected to promote and manage the facilities helpdesk, assist with regulatory site in...... click apply for full job details
A great interim job opportunity to join and established HR team within the NHS. Your new role In your new role you will: Produce accurate and timely analytical and statistical workforce report using key data sources from by use of the Oracle Discoverer and other sources of workforce information, Identify trends relating to talent (appraisal data), staff development (training needs), recruitment and re...... click apply for full job details
Dec 02, 2020
Seasonal
A great interim job opportunity to join and established HR team within the NHS. Your new role In your new role you will: Produce accurate and timely analytical and statistical workforce report using key data sources from by use of the Oracle Discoverer and other sources of workforce information, Identify trends relating to talent (appraisal data), staff development (training needs), recruitment and re...... click apply for full job details
British Antarctic Survey
Cambridge, Cambridgeshire
Due to the COVID-19 outbreak, please note there may be delays to our recruitment timeline. We are looking for an Administrator to provide support to our Stations in Antarctica. The role will be based in Cambridge, UK. British Antarctic Survey (BAS) delivers and enables world-leading interdisciplinary research in the Polar Regions...... click apply for full job details
Dec 02, 2020
Contractor
Due to the COVID-19 outbreak, please note there may be delays to our recruitment timeline. We are looking for an Administrator to provide support to our Stations in Antarctica. The role will be based in Cambridge, UK. British Antarctic Survey (BAS) delivers and enables world-leading interdisciplinary research in the Polar Regions...... click apply for full job details
Interim Senior Workforce Analyst to join an established team within the NHS for at least 3 months Your new role Provide insightful analysis, identify relationship and emerging trends and predict future workforce trends from disparate sources to support data-driven management strategies Ensure accurate workforce report is available at all levels of the organisation...... click apply for full job details
Dec 02, 2020
Seasonal
Interim Senior Workforce Analyst to join an established team within the NHS for at least 3 months Your new role Provide insightful analysis, identify relationship and emerging trends and predict future workforce trends from disparate sources to support data-driven management strategies Ensure accurate workforce report is available at all levels of the organisation...... click apply for full job details
*Statistical Programmers - Senior / Principal, Early Biometrics & Statistical Innovation * Are you a goal-oriented Statistical Programmer looking for a new challenge? Would you like to be a part of a group with direct strategic impact on drug development that plays a key role in getting new medicines to patients who need them? Welcome to join AstraZeneca with your expertise! We are currently recruiting Statistical Programmer at senior level or higher depending on your previous experience to join our growing Early stage portfolio. Our main therapy areas are Cardiovascular, Renal, and Metabolism (CVRM) and Respiratory & Immunology (R&I). The positions can either be based in *Cambridge, UK.* *Description* At AstraZeneca we're driving leading-edge approaches to drug development across many business areas - within Early Biometrics & Statistical Innovation (EB&SI) a data-centric focus is helping us work more efficiently and creatively to bring the right medicines to the right patients. Our biometrics teams use their expertise in statistics and programming to answer drug development objectives and reduce uncertainty in product development, driving better business decisions with quantitative reasoning. The Senior/Principal Programmer sits within our Early Programming group in EB&SI, aligned either to Cardiovascular/ Renal/ Metabolism (CVRM) or Respiratory, Inflammation, and Autoimmunity (R&I), and is responsible for providing statistical programming expertise to support the design and interpretation of early clinical studies and development programmes. Working as part of Data Science and AI, you'll be able to access technology at the forefront of science in an innovative environment, where you will have scope to develop creative statistical ideas and approaches, and to apply them in your work. *Main duties and responsibilities* The Senior/Principal Programmer provide Statistical Programming support and/or lead all programming related activities of the analysis and reporting process including, but not limited to, CSR development, regulatory activities and the scientific utilization of our data for AstraZeneca products. There are many career options you can pursue for progression including technical pathways, management of global projects or line management. You will work in the Programming department that not only oversees and delivers the programming aspects of analysis and reporting but also manages and maintains our end-to-end standards and our analysis and reporting production tools. You'll be part of a global team that pulls together to put patients first. *Requirements* To succeed in this role, you'll be an experienced programmer with good knowledge of technical and regulatory requirements related to programming within the pharmaceutical or healthcare industry. You'll enjoy multitasking, have an appetite for solving problems with a strong team focus who enjoys collaborating to achieve the best results. We have several opportunities across both Senior and Principal levels. Desirable experience includes: Both * BSc in a Mathematical (i.e. Applied Math, Engineering, etc.), Statistical, Computer Science or Life Science subject * Excellent problem-solving skills * Diligence - attention to detail and ability to manage concurrent projects and activities * Excellent verbal and written communication skills and ability to influence stakeholders Senior * SAS programming expertise gained within a clinical drug development or healthcare setting * Knowledge of CDISC standards and industry best practices * Knowledge of database set-up and report publishing requirements Principal * Extensive SAS programming expertise to an advanced level * Extensive Knowledge of Analysis and Reporting within Clinical Development * Comprehensive knowledge of technical and regulatory requirements with submission experience * Wide-ranging knowledge of CDISC standards and industry best practices * Travel - willingness and ability to travel domestically and/or internationally * Team centric approach: keen to take steps to understand and appreciate the roles, skills and strengths of others on the team *More information* For more information about these positions please contact Catherine Rochez [ ](mailto: ) Pontus Boman [ ](mailto: ) For more information, please visit our websites: Gothenburg site: []() Cambridge site: []() Gaithersburg site: []()
Dec 02, 2020
Full time
*Statistical Programmers - Senior / Principal, Early Biometrics & Statistical Innovation * Are you a goal-oriented Statistical Programmer looking for a new challenge? Would you like to be a part of a group with direct strategic impact on drug development that plays a key role in getting new medicines to patients who need them? Welcome to join AstraZeneca with your expertise! We are currently recruiting Statistical Programmer at senior level or higher depending on your previous experience to join our growing Early stage portfolio. Our main therapy areas are Cardiovascular, Renal, and Metabolism (CVRM) and Respiratory & Immunology (R&I). The positions can either be based in *Cambridge, UK.* *Description* At AstraZeneca we're driving leading-edge approaches to drug development across many business areas - within Early Biometrics & Statistical Innovation (EB&SI) a data-centric focus is helping us work more efficiently and creatively to bring the right medicines to the right patients. Our biometrics teams use their expertise in statistics and programming to answer drug development objectives and reduce uncertainty in product development, driving better business decisions with quantitative reasoning. The Senior/Principal Programmer sits within our Early Programming group in EB&SI, aligned either to Cardiovascular/ Renal/ Metabolism (CVRM) or Respiratory, Inflammation, and Autoimmunity (R&I), and is responsible for providing statistical programming expertise to support the design and interpretation of early clinical studies and development programmes. Working as part of Data Science and AI, you'll be able to access technology at the forefront of science in an innovative environment, where you will have scope to develop creative statistical ideas and approaches, and to apply them in your work. *Main duties and responsibilities* The Senior/Principal Programmer provide Statistical Programming support and/or lead all programming related activities of the analysis and reporting process including, but not limited to, CSR development, regulatory activities and the scientific utilization of our data for AstraZeneca products. There are many career options you can pursue for progression including technical pathways, management of global projects or line management. You will work in the Programming department that not only oversees and delivers the programming aspects of analysis and reporting but also manages and maintains our end-to-end standards and our analysis and reporting production tools. You'll be part of a global team that pulls together to put patients first. *Requirements* To succeed in this role, you'll be an experienced programmer with good knowledge of technical and regulatory requirements related to programming within the pharmaceutical or healthcare industry. You'll enjoy multitasking, have an appetite for solving problems with a strong team focus who enjoys collaborating to achieve the best results. We have several opportunities across both Senior and Principal levels. Desirable experience includes: Both * BSc in a Mathematical (i.e. Applied Math, Engineering, etc.), Statistical, Computer Science or Life Science subject * Excellent problem-solving skills * Diligence - attention to detail and ability to manage concurrent projects and activities * Excellent verbal and written communication skills and ability to influence stakeholders Senior * SAS programming expertise gained within a clinical drug development or healthcare setting * Knowledge of CDISC standards and industry best practices * Knowledge of database set-up and report publishing requirements Principal * Extensive SAS programming expertise to an advanced level * Extensive Knowledge of Analysis and Reporting within Clinical Development * Comprehensive knowledge of technical and regulatory requirements with submission experience * Wide-ranging knowledge of CDISC standards and industry best practices * Travel - willingness and ability to travel domestically and/or internationally * Team centric approach: keen to take steps to understand and appreciate the roles, skills and strengths of others on the team *More information* For more information about these positions please contact Catherine Rochez [ ](mailto: ) Pontus Boman [ ](mailto: ) For more information, please visit our websites: Gothenburg site: []() Cambridge site: []() Gaithersburg site: []()
*About Us* Since the global network was founded in 1952 by a family of physicians, the Mundipharma network has always challenged conventional wisdom, and we expect the same from our employees. If you crave the freedom to think and work in new ways, then this is the place for you. Our flat organization allows you to make decisions and deliver results fast, which makes this an exhilarating and exciting place to work regardless of your role. *Job Description* Responsible for providing global regulatory strategic leadership for assigned marketed products. Responsible for Regulatory oversight for the outsourced activities linked to the assigned marketed products. *Duties & Responsibilities* * Responsible for assigned marketed products including global regulatory strategy and execution. * Engagement with stakeholders and partners across the Mundipharma business for provision of Regulatory Strategy advice and expertise for the assigned Marketed products. * Responsible for ensuring quality delivery from vendors in line with agreed asset strategy. * Provide regulatory expertise for the assigned marketed products. * Act as Regulatory Lead and engage with stakeholders across the organisation to understand strategic and commercial goals for the assigned marketed products. * Provide ownership and accountability for timely and effective regulatory strategy and execution for the assigned marketed products. * Provision of strategic direction and oversight of delivery output from outsourcing partners to ensure alignment with regulatory strategies, effective execution and quality submissions. * Responsible for regulatory representation in Alliance Management with Partner companies for their assigned marketed products, where applicable. * Provision of marketed products regulatory expertise into assigned Due Diligence. * Ensure that regulatory strategies for the assigned Marketed Products fully recognise risk, provide mitigations and ensure that these are communicated and acknowledged within the organisation for appropriate commercial decision-making * Responsible agency negotiations and interactions for assigned Marketed Products where appropriate *Who we're looking for* * Extensive regulatory experience in registration and maintenance of products globally. * Excellent knowledge and understanding of Emerging Markets regulatory requirements. * Proven track-record of oversight and delivery of successful regulatory outcomes for marketed products across multiple regions. * Strong negotiation and problem-solving skills, self-motivated, driven with a positive attitude. * Leading agency negotiations and interactions for Marketed products where appropriate. * Excellent communication skills and ability to engage with Senior Leaders within the organisation effectively. * Strong collaborator with excellent stakeholder and customer focus. * Ability to work effectively within a flexible resourcing environment harnessing both internal and external (outsourcing) providers to deliver regulatory results. *Do you think you could help us see what others don't? Be inquisitive and help us move medicine forward!*
Dec 02, 2020
Full time
*About Us* Since the global network was founded in 1952 by a family of physicians, the Mundipharma network has always challenged conventional wisdom, and we expect the same from our employees. If you crave the freedom to think and work in new ways, then this is the place for you. Our flat organization allows you to make decisions and deliver results fast, which makes this an exhilarating and exciting place to work regardless of your role. *Job Description* Responsible for providing global regulatory strategic leadership for assigned marketed products. Responsible for Regulatory oversight for the outsourced activities linked to the assigned marketed products. *Duties & Responsibilities* * Responsible for assigned marketed products including global regulatory strategy and execution. * Engagement with stakeholders and partners across the Mundipharma business for provision of Regulatory Strategy advice and expertise for the assigned Marketed products. * Responsible for ensuring quality delivery from vendors in line with agreed asset strategy. * Provide regulatory expertise for the assigned marketed products. * Act as Regulatory Lead and engage with stakeholders across the organisation to understand strategic and commercial goals for the assigned marketed products. * Provide ownership and accountability for timely and effective regulatory strategy and execution for the assigned marketed products. * Provision of strategic direction and oversight of delivery output from outsourcing partners to ensure alignment with regulatory strategies, effective execution and quality submissions. * Responsible for regulatory representation in Alliance Management with Partner companies for their assigned marketed products, where applicable. * Provision of marketed products regulatory expertise into assigned Due Diligence. * Ensure that regulatory strategies for the assigned Marketed Products fully recognise risk, provide mitigations and ensure that these are communicated and acknowledged within the organisation for appropriate commercial decision-making * Responsible agency negotiations and interactions for assigned Marketed Products where appropriate *Who we're looking for* * Extensive regulatory experience in registration and maintenance of products globally. * Excellent knowledge and understanding of Emerging Markets regulatory requirements. * Proven track-record of oversight and delivery of successful regulatory outcomes for marketed products across multiple regions. * Strong negotiation and problem-solving skills, self-motivated, driven with a positive attitude. * Leading agency negotiations and interactions for Marketed products where appropriate. * Excellent communication skills and ability to engage with Senior Leaders within the organisation effectively. * Strong collaborator with excellent stakeholder and customer focus. * Ability to work effectively within a flexible resourcing environment harnessing both internal and external (outsourcing) providers to deliver regulatory results. *Do you think you could help us see what others don't? Be inquisitive and help us move medicine forward!*
Title: Regulatory Affairs Manager - CMC Europe Duration: 12 Months Location: Cambridge or Uxbridge or Remote WFH - flex to work across either site, but Cambridge is the preferred site (post covid still flex to WFH) Looking for a L5 Reg Affairs CMC We need someone has provided general support for EU/Swiss variations Experience of emerging markets Russia/Balkans Carrying out change assessments Interaction with multiply stakeholders, Reg affairs operations Clinical (CTA) experience is less important, candidates must have POST APPROVAL experience Ideally will come from a big pharma/biologic experience Personal that can work independently Ideally 5 + years in a similar level role This role will be more broader so candidates with experience/at least a knowledge of the full life cycle will really stand out Job Description: The company: Client is one of the world's leading independent biotechnology companies, and has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Client has not only discovered and developed innovative human therapeutics, but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. The role: The Regulatory Professional will play a key role in developing and executing CMC regulatory strategies for new marketing authorisation applications and throughout whole product life cycle for the European (EU and Switzerland) and Extended European region (Balkans, Israel, Russia) Responsibilities will include: Ensuring CMC regional issues impacting global regulatory strategy for proposed CMC filings are considered and risks identified with appropriate contingency strategies Review the preparation of M2 and 3 CMC components of filings and assess fitness of purpose for submission in the relevant countries Manages Strategy and Execution for all regulatory submissions (eg clinical trial and variations) Authoring and coordinating responses to questions across assigned products and countries. Point of Contact with local country regulatory staff Project management of submissions and monitoring status of applications Communicate regional needs for ensuring reliability of the supply chain and successful launch are well defined and implemented in collaboration with relevant regional stakeholders Ensure regulatory product compliance for product (eg IMR, PMCs, paediatric and other agency commitments) Share regulatory information and implications with the stakeholders on an ongoing basis and provide advice on regional considerations Performs regulatory research to obtain relevant histories, precedence and other information relevant to regional product advancement. Provides guidance for regulatory assessments of change control requests Sets project timeframes and priorities for products under their responsibility based on project objectives and ongoing assignments; raises resource constraints Document and communicate details and outcomes of regulatory agency interactions to global regulatory and operations teams and relevant sr. management Knowledge and Skills: Regulatory knowledge in regional legislation Working with policies, procedures and SOPs Experience with national legislation and regulations relating to medicinal products Understanding of the regional regulatory procedures for CTAs, MAs, post approval changes, extensions and renewals. Understanding of drug development Scientific/Technical Excellence Strong knowledge of and experience in regional regulatory environment in relevant product area and development stage Ability to resolve conflicts and develop a course of action leading to a beneficial outcome Cultural awareness and sensitivity to achieve results across both regional country and International borders. Strong team player with a commitment to customer service In-depth experience of pharmaceutical/biotechnology or medical device industry Strong record of related experience within Regulatory Affairs (min 5 years) Strong communication skills - oral and written Organizational skills Strong interpersonal skills Ability to develop solutions to technical and organizational issues in order to improve performance and productivity Strong computer skills, including word processing, database document repository and project management software Attention to detail Relationship building Ability to work well with others in demanding situations with a positive attitude demonstrating tact, diplomacy and respect Time and project management skills Problem solving Prioritisation Ability to work in a fast paced environment
Dec 02, 2020
Contractor
Title: Regulatory Affairs Manager - CMC Europe Duration: 12 Months Location: Cambridge or Uxbridge or Remote WFH - flex to work across either site, but Cambridge is the preferred site (post covid still flex to WFH) Looking for a L5 Reg Affairs CMC We need someone has provided general support for EU/Swiss variations Experience of emerging markets Russia/Balkans Carrying out change assessments Interaction with multiply stakeholders, Reg affairs operations Clinical (CTA) experience is less important, candidates must have POST APPROVAL experience Ideally will come from a big pharma/biologic experience Personal that can work independently Ideally 5 + years in a similar level role This role will be more broader so candidates with experience/at least a knowledge of the full life cycle will really stand out Job Description: The company: Client is one of the world's leading independent biotechnology companies, and has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Client has not only discovered and developed innovative human therapeutics, but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. The role: The Regulatory Professional will play a key role in developing and executing CMC regulatory strategies for new marketing authorisation applications and throughout whole product life cycle for the European (EU and Switzerland) and Extended European region (Balkans, Israel, Russia) Responsibilities will include: Ensuring CMC regional issues impacting global regulatory strategy for proposed CMC filings are considered and risks identified with appropriate contingency strategies Review the preparation of M2 and 3 CMC components of filings and assess fitness of purpose for submission in the relevant countries Manages Strategy and Execution for all regulatory submissions (eg clinical trial and variations) Authoring and coordinating responses to questions across assigned products and countries. Point of Contact with local country regulatory staff Project management of submissions and monitoring status of applications Communicate regional needs for ensuring reliability of the supply chain and successful launch are well defined and implemented in collaboration with relevant regional stakeholders Ensure regulatory product compliance for product (eg IMR, PMCs, paediatric and other agency commitments) Share regulatory information and implications with the stakeholders on an ongoing basis and provide advice on regional considerations Performs regulatory research to obtain relevant histories, precedence and other information relevant to regional product advancement. Provides guidance for regulatory assessments of change control requests Sets project timeframes and priorities for products under their responsibility based on project objectives and ongoing assignments; raises resource constraints Document and communicate details and outcomes of regulatory agency interactions to global regulatory and operations teams and relevant sr. management Knowledge and Skills: Regulatory knowledge in regional legislation Working with policies, procedures and SOPs Experience with national legislation and regulations relating to medicinal products Understanding of the regional regulatory procedures for CTAs, MAs, post approval changes, extensions and renewals. Understanding of drug development Scientific/Technical Excellence Strong knowledge of and experience in regional regulatory environment in relevant product area and development stage Ability to resolve conflicts and develop a course of action leading to a beneficial outcome Cultural awareness and sensitivity to achieve results across both regional country and International borders. Strong team player with a commitment to customer service In-depth experience of pharmaceutical/biotechnology or medical device industry Strong record of related experience within Regulatory Affairs (min 5 years) Strong communication skills - oral and written Organizational skills Strong interpersonal skills Ability to develop solutions to technical and organizational issues in order to improve performance and productivity Strong computer skills, including word processing, database document repository and project management software Attention to detail Relationship building Ability to work well with others in demanding situations with a positive attitude demonstrating tact, diplomacy and respect Time and project management skills Problem solving Prioritisation Ability to work in a fast paced environment
*About Us* Since the global network was founded in 1952 by a family of physicians, the Mundipharma network has always challenged conventional wisdom, and we expect the same from our employees. If you crave the freedom to think and work in new ways, then this is the place for you. Our flat organization allows you to make decisions and deliver results fast, which makes this an exhilarating and exciting place to work regardless of your role. *Job Description* To oversee statistical and programming activities for clinical data studies performed by external vendors while also providing additional consultancy and implementation of data driven solutions and insights to internal stakeholders. Responsible for presenting the real value of data science working across Mundipharma functions to make data driven decisions by identifying potential research areas; these may include clinical trial data, real world data (primary/secondary) and the use of advanced analytics and modelling and simulation techniques. In addition, to design and implement software solutions to aid data visualisation, access and interpretation, and input into Mundipharma process improvements and external initiatives. *Duties & Responsibilities* * Expertise in the use of statistics and programming/software development to design and analyse clinical trial data, real world data studies/analysis and develop innovative trial designs. * Provide statistical and programming input into clinical study design, real world evidence data capture and analyses, and advanced software solutions including data visualisation using software such as SAS, R and Python. * Vendor oversight for optimum database design and analysis delivery to provide cost efficient solutions to Mundipharma. * Responsible for the delivery of clinical studies and specific study related deliverables working across a matrix organisation with external oversight of CROs and consultants. * To deliver on internal projects related to research areas of interest aligned with R&D objectives. * Day to day decisions for managing clinical studies and other data sources with alignment of other key functions and budget holders. * Significantly input into the development of process improvements within Data Science, maintain up to date knowledge of external guidelines, industry standards and technology. * Externally represent Mundipharma at conferences and industry-wide initiatives. *Who we're looking for* * Experience in the application of programming and statistics in the drug development process particularly related to the simplification of complex data structures from multiple sources, into interpretable and analysable forms using a core data model approach. * Experience in the use of advanced analytical techniques and the development of data visualisation tools using SAS, R and/or Python. * Experience of database design and EDC systems and other data capture (e.g. EDC, PROs, Real World Data, analytics, eMobile, EHR) as well as the ability to interrogate data logically and assess data quality. * Experience of delivering clinical studies across multiple phases and therapeutic areas including primary and secondary data sources; experience of successfully managing different vendors. * Proven ability to perform self-motivated research using clinical trial data and/or real-world data with the aptitude to provide convincing evidence to influence decisions. * Ability to work cross functionally, interpret information and critically assess performance of external consultants and CROs. * Ability to prioritise, work flexibly and think strategically. * Familiar with the regulatory landscape and required data standards. *Do you think you could help us see what others don't? Be inquisitive and help us move medicine forward!*
Dec 02, 2020
Full time
*About Us* Since the global network was founded in 1952 by a family of physicians, the Mundipharma network has always challenged conventional wisdom, and we expect the same from our employees. If you crave the freedom to think and work in new ways, then this is the place for you. Our flat organization allows you to make decisions and deliver results fast, which makes this an exhilarating and exciting place to work regardless of your role. *Job Description* To oversee statistical and programming activities for clinical data studies performed by external vendors while also providing additional consultancy and implementation of data driven solutions and insights to internal stakeholders. Responsible for presenting the real value of data science working across Mundipharma functions to make data driven decisions by identifying potential research areas; these may include clinical trial data, real world data (primary/secondary) and the use of advanced analytics and modelling and simulation techniques. In addition, to design and implement software solutions to aid data visualisation, access and interpretation, and input into Mundipharma process improvements and external initiatives. *Duties & Responsibilities* * Expertise in the use of statistics and programming/software development to design and analyse clinical trial data, real world data studies/analysis and develop innovative trial designs. * Provide statistical and programming input into clinical study design, real world evidence data capture and analyses, and advanced software solutions including data visualisation using software such as SAS, R and Python. * Vendor oversight for optimum database design and analysis delivery to provide cost efficient solutions to Mundipharma. * Responsible for the delivery of clinical studies and specific study related deliverables working across a matrix organisation with external oversight of CROs and consultants. * To deliver on internal projects related to research areas of interest aligned with R&D objectives. * Day to day decisions for managing clinical studies and other data sources with alignment of other key functions and budget holders. * Significantly input into the development of process improvements within Data Science, maintain up to date knowledge of external guidelines, industry standards and technology. * Externally represent Mundipharma at conferences and industry-wide initiatives. *Who we're looking for* * Experience in the application of programming and statistics in the drug development process particularly related to the simplification of complex data structures from multiple sources, into interpretable and analysable forms using a core data model approach. * Experience in the use of advanced analytical techniques and the development of data visualisation tools using SAS, R and/or Python. * Experience of database design and EDC systems and other data capture (e.g. EDC, PROs, Real World Data, analytics, eMobile, EHR) as well as the ability to interrogate data logically and assess data quality. * Experience of delivering clinical studies across multiple phases and therapeutic areas including primary and secondary data sources; experience of successfully managing different vendors. * Proven ability to perform self-motivated research using clinical trial data and/or real-world data with the aptitude to provide convincing evidence to influence decisions. * Ability to work cross functionally, interpret information and critically assess performance of external consultants and CROs. * Ability to prioritise, work flexibly and think strategically. * Familiar with the regulatory landscape and required data standards. *Do you think you could help us see what others don't? Be inquisitive and help us move medicine forward!*
EXPERIENCED SALES VALUER/LISTER Company description Offering a new approach to Estate Agency. Flexible working from home, manage your own time, fantastic people, realistic ability to earn your worth! Job description We're looking for outstanding, proven residential sales valuers to join this progressive team and truly earn their worth...... click apply for full job details
Dec 02, 2020
Full time
EXPERIENCED SALES VALUER/LISTER Company description Offering a new approach to Estate Agency. Flexible working from home, manage your own time, fantastic people, realistic ability to earn your worth! Job description We're looking for outstanding, proven residential sales valuers to join this progressive team and truly earn their worth...... click apply for full job details
Clinical Data Management Project Manager (CDM PM) - EMEA Home Based We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD - thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. Are you a data and a people person? Here's your team. We manage and clean the data collected in a clinical trial - from the design and build of the database and edit checks, through the entry and cleaning of data to the final delivery of clinical trial data. We work closely with the project teams and clients to identify best practices and processes, meet and exceed our clients' needs, and do the right thing to earn their trust. As a Clinical Data Management Project Manager, you will help ensure the highest quality of data and effectiveness of CDM Projects. You will work directly with management to manage CDM projects including ownership of financials of projects. This position works closely with clients and other team members at PPD. At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. Summarized Purpose: In this role you will act as a study manager for multiple studies individually or as a program of several studies. You may perform the Project Manager role for standalone studies. You will be responsible for functional, administrative and financial oversight of assigned projects. Essential Functions: * Provides support and coaching to the DM team to ensure that all tasks are completed accurately, on time and within budget to meet or exceed client expectations. * Acts as a primary liaison for project team and client. * May develop and implement study specific training for DM project staff and performs independent reviews of DM deliverables following CDM guidelines. * Monitors, evaluates and proposes mitigation strategies surrounding risk to deliverables and finances. Participates in business development activities by assisting with bid preparation and representing data management at bid defense meetings, where required. Additionally, promotes repeat business by developing relationships with new and existing clients. * Performs project forecasting of hours and identification of resource requirements and manages project budgets including identification of out of scope work and participate in the Contract Modification process. * Participates in the development and implementation of processes, procedures and training for the data management function as directed. * Mentors junior level staff and peers on all associated tasks within a study or program. * Independently leads and delegates tasks to ensure timely completion of project activities to project timelines, quality and budget. *Qualifications:* Education/Experience: Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8 + years). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills & Abilities: * Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations * Ability to use interactive computer programs * Excellent written/ verbal communication skills with a strong command of English language and grammar; strong organizational and analytical/problem solving skills; strong customer focus and excellent interpersonal skills * Ability to identify project risks and to effectively evaluate and develop plans to mitigate those risks * Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data * Ability to act as a study or department expert for DM processes. * Ability to train and direct a study team, providing leadership and direction to both subordinates and peers * Ability to forecast project resourcing, project timeline planning and adherence to timelines. * Ability to supervise and delegate tasks. * Ability to successfully apply above skills, knowledge and abilities across a portfolio of studies" PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. This position may require travel. 10-20% annual possible. PPD Defining Principles: - We have a strong will to win - We earn our customer's trust - We are gamechangers - We do the right thing - We are one PPD - If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, then please submit your application - we'd love to hear from you *LI-SH1
Dec 02, 2020
Full time
Clinical Data Management Project Manager (CDM PM) - EMEA Home Based We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD - thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. Are you a data and a people person? Here's your team. We manage and clean the data collected in a clinical trial - from the design and build of the database and edit checks, through the entry and cleaning of data to the final delivery of clinical trial data. We work closely with the project teams and clients to identify best practices and processes, meet and exceed our clients' needs, and do the right thing to earn their trust. As a Clinical Data Management Project Manager, you will help ensure the highest quality of data and effectiveness of CDM Projects. You will work directly with management to manage CDM projects including ownership of financials of projects. This position works closely with clients and other team members at PPD. At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. Summarized Purpose: In this role you will act as a study manager for multiple studies individually or as a program of several studies. You may perform the Project Manager role for standalone studies. You will be responsible for functional, administrative and financial oversight of assigned projects. Essential Functions: * Provides support and coaching to the DM team to ensure that all tasks are completed accurately, on time and within budget to meet or exceed client expectations. * Acts as a primary liaison for project team and client. * May develop and implement study specific training for DM project staff and performs independent reviews of DM deliverables following CDM guidelines. * Monitors, evaluates and proposes mitigation strategies surrounding risk to deliverables and finances. Participates in business development activities by assisting with bid preparation and representing data management at bid defense meetings, where required. Additionally, promotes repeat business by developing relationships with new and existing clients. * Performs project forecasting of hours and identification of resource requirements and manages project budgets including identification of out of scope work and participate in the Contract Modification process. * Participates in the development and implementation of processes, procedures and training for the data management function as directed. * Mentors junior level staff and peers on all associated tasks within a study or program. * Independently leads and delegates tasks to ensure timely completion of project activities to project timelines, quality and budget. *Qualifications:* Education/Experience: Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8 + years). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills & Abilities: * Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations * Ability to use interactive computer programs * Excellent written/ verbal communication skills with a strong command of English language and grammar; strong organizational and analytical/problem solving skills; strong customer focus and excellent interpersonal skills * Ability to identify project risks and to effectively evaluate and develop plans to mitigate those risks * Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data * Ability to act as a study or department expert for DM processes. * Ability to train and direct a study team, providing leadership and direction to both subordinates and peers * Ability to forecast project resourcing, project timeline planning and adherence to timelines. * Ability to supervise and delegate tasks. * Ability to successfully apply above skills, knowledge and abilities across a portfolio of studies" PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. This position may require travel. 10-20% annual possible. PPD Defining Principles: - We have a strong will to win - We earn our customer's trust - We are gamechangers - We do the right thing - We are one PPD - If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, then please submit your application - we'd love to hear from you *LI-SH1
A new exciting opportunity has come up as a Technical Support Advisor with a top supplier and manufacturer of laboratory products. This is a great opportunity for someone with a scientific background and customer support experience! This role forms part of the central customer support team which is the hub of business...... click apply for full job details
Dec 02, 2020
Full time
A new exciting opportunity has come up as a Technical Support Advisor with a top supplier and manufacturer of laboratory products. This is a great opportunity for someone with a scientific background and customer support experience! This role forms part of the central customer support team which is the hub of business...... click apply for full job details
Automotive Security Engineer Cambridge to £50k Automotive Security Engineer (CAN ICE Ethernet). World-leading cyber security organisation is seeking a standout technologist to take the lead role in the R&D product development for a ground-breaking automotive security product. The ideal candidate will have a wealth of all round automotive-in vehicle experience, from CAN networks at one end, to kn...... click apply for full job details
Dec 01, 2020
Full time
Automotive Security Engineer Cambridge to £50k Automotive Security Engineer (CAN ICE Ethernet). World-leading cyber security organisation is seeking a standout technologist to take the lead role in the R&D product development for a ground-breaking automotive security product. The ideal candidate will have a wealth of all round automotive-in vehicle experience, from CAN networks at one end, to kn...... click apply for full job details
CK Group are recruiting for a RWE Statistician to join a company in the Pharmaceutical industry at their site based in Cambridge on a contract basis for 6 months. *Company:* Our client is a global pharmaceutical company with a major presence in the UK. Their purpose is to deliver life-changing medicines and to do this they are completely science-led and like to share this with the scientific, healthcare and business communities within the UK. *Location:* This RWE Statistician role will be based at our clients site in Cambridge. *Salary:* Up to £600 per day DOE. *RWE Statistician Role:* * Provide statistical expertise in the design, analysis and interpretation of secondary observational research studies/IVS contracts and primary data collection clinical studies/trials in support of BioPharmaceuticals Medical & Payer evidence generation research activities. * Provide expert advice in the analysis of real world data (such as medical claims, electronic health records, registries) for stakeholders. * Collaborate in the development of operational systems and research processes to increase the effectiveness and efficiency of BPM Evidence and RWS&D research efforts. *Your Background:* * Graduate degree in Statistics, Biostatistics, or related quantitative fields, or equivalent working experience within the pharmaceutical industries. * Experience in the design, analysis and reporting of clinical studies/trials in a pharmaceutical research or academic setting. * Experience using RWE Analytic Tools & platforms (e.g., IHD/Aetion Analytic tools). * Proficiency in SAS, SQL and/or R. * Experience working with large healthcare claims and EMR databases such as Truven MarketScan, Optum, CPRD or similar. *Apply:* Quote job ref 49113. It is essential that applicants hold entitlement to work in the UK. CLINGEN
Dec 01, 2020
Full time
CK Group are recruiting for a RWE Statistician to join a company in the Pharmaceutical industry at their site based in Cambridge on a contract basis for 6 months. *Company:* Our client is a global pharmaceutical company with a major presence in the UK. Their purpose is to deliver life-changing medicines and to do this they are completely science-led and like to share this with the scientific, healthcare and business communities within the UK. *Location:* This RWE Statistician role will be based at our clients site in Cambridge. *Salary:* Up to £600 per day DOE. *RWE Statistician Role:* * Provide statistical expertise in the design, analysis and interpretation of secondary observational research studies/IVS contracts and primary data collection clinical studies/trials in support of BioPharmaceuticals Medical & Payer evidence generation research activities. * Provide expert advice in the analysis of real world data (such as medical claims, electronic health records, registries) for stakeholders. * Collaborate in the development of operational systems and research processes to increase the effectiveness and efficiency of BPM Evidence and RWS&D research efforts. *Your Background:* * Graduate degree in Statistics, Biostatistics, or related quantitative fields, or equivalent working experience within the pharmaceutical industries. * Experience in the design, analysis and reporting of clinical studies/trials in a pharmaceutical research or academic setting. * Experience using RWE Analytic Tools & platforms (e.g., IHD/Aetion Analytic tools). * Proficiency in SAS, SQL and/or R. * Experience working with large healthcare claims and EMR databases such as Truven MarketScan, Optum, CPRD or similar. *Apply:* Quote job ref 49113. It is essential that applicants hold entitlement to work in the UK. CLINGEN
About Us Since the global network was founded in 1952 by a family of physicians, the Mundipharma network has always challenged conventional wisdom, and we expect the same from our employees. If you crave the freedom to think and work in new ways, then this is the place for you. Our flat organization allows you to make decisions and deliver results fast, which makes this an exhilarating and exciting...... click apply for full job details
Dec 01, 2020
Full time
About Us Since the global network was founded in 1952 by a family of physicians, the Mundipharma network has always challenged conventional wisdom, and we expect the same from our employees. If you crave the freedom to think and work in new ways, then this is the place for you. Our flat organization allows you to make decisions and deliver results fast, which makes this an exhilarating and exciting...... click apply for full job details
Job Family: Support Worker Location: Cambridge, Cambridgeshire Pay Rate (£): £9.04 per hour Vacancy Reference: 025451 Experienced Support WorkersSuez Road, CB1Full/Part Time AvailableFull driving licence essentialOffering up to £1,422 per monthJoin us to help provide the best care possible to individuals with learning disabilities to live the most independent and fulfilled lives that we can support.Working with Voyage Care you will receive full training, competitive benefits packages, supported career progression and a great team. Suez Road is 2 properties supporting individuals with living their lives on a daily basis. Each individual at Suez Road that we support has their own unique personality and when able they are all actively out in the community taking part in a variety of different activities such as swimming and going to the cinema.This position is full/part time, covering shifts throughout the week and some nights on a rotational shift basis (0, 1 & 2).We truly believe that by helping individuals with the everyday challenges of washing, dressing, eating and regular activities, that you'll enable them to do the things that most people take for granted.This is a fantastic opportunity to join a growing organisation who truly put those we support at the heart of our business.COVID19 safety is important to us all, we support our staff and the people we support to stay safe by wearing correct PPE, including Type IIR Fluid Resistant Surgical Masks (FRSM), aprons and gloves at all times. We have a in-house team that ensures that all of our services have plenty of PPE at all times. All care and support is carried out following the latest Government guidance. Our aim is to keep you and the people we support safe.If you are interested in this role and would like to find out more, please contact Shane on or click apply. Benefits: We invest in a wide range of benefits to reward our Support Workers for the brilliant job they do. We offer a pension scheme; retail discount package with some great offers, including holiday discounts to gym membership; our employee assistance programme offers independent advice and support 24 hours a day. About Voyage Care: We are passionate about caring for our people. You'll be working with a company that is renowned for treating people properly and providing a training, development, compliance and support structure that simply can't be found anywhere else. We are committed to delivering quality care and that's why our care homes have a quality score of 96%, practically unheard of in our industry. As part of a passionate, close-knit team there will always be someone on hand to help you out. To be part of our Voyage Care family, please click to apply via email or give us a call on We are committed to safeguarding and promoting the welfare of the people we support. All successful candidates will be subject to an Enhanced DBS/PVG check and Regulated Activity which will include a check against the Barred adult list. * Some of our roles require male or female employees only, where this is indicated it is a genuine occupational requirement, in accordance with the Equality Act 2010 Role Specific Requirements - Driver: Driver Required Gender: No Specific Requirement
Dec 01, 2020
Full time
Job Family: Support Worker Location: Cambridge, Cambridgeshire Pay Rate (£): £9.04 per hour Vacancy Reference: 025451 Experienced Support WorkersSuez Road, CB1Full/Part Time AvailableFull driving licence essentialOffering up to £1,422 per monthJoin us to help provide the best care possible to individuals with learning disabilities to live the most independent and fulfilled lives that we can support.Working with Voyage Care you will receive full training, competitive benefits packages, supported career progression and a great team. Suez Road is 2 properties supporting individuals with living their lives on a daily basis. Each individual at Suez Road that we support has their own unique personality and when able they are all actively out in the community taking part in a variety of different activities such as swimming and going to the cinema.This position is full/part time, covering shifts throughout the week and some nights on a rotational shift basis (0, 1 & 2).We truly believe that by helping individuals with the everyday challenges of washing, dressing, eating and regular activities, that you'll enable them to do the things that most people take for granted.This is a fantastic opportunity to join a growing organisation who truly put those we support at the heart of our business.COVID19 safety is important to us all, we support our staff and the people we support to stay safe by wearing correct PPE, including Type IIR Fluid Resistant Surgical Masks (FRSM), aprons and gloves at all times. We have a in-house team that ensures that all of our services have plenty of PPE at all times. All care and support is carried out following the latest Government guidance. Our aim is to keep you and the people we support safe.If you are interested in this role and would like to find out more, please contact Shane on or click apply. Benefits: We invest in a wide range of benefits to reward our Support Workers for the brilliant job they do. We offer a pension scheme; retail discount package with some great offers, including holiday discounts to gym membership; our employee assistance programme offers independent advice and support 24 hours a day. About Voyage Care: We are passionate about caring for our people. You'll be working with a company that is renowned for treating people properly and providing a training, development, compliance and support structure that simply can't be found anywhere else. We are committed to delivering quality care and that's why our care homes have a quality score of 96%, practically unheard of in our industry. As part of a passionate, close-knit team there will always be someone on hand to help you out. To be part of our Voyage Care family, please click to apply via email or give us a call on We are committed to safeguarding and promoting the welfare of the people we support. All successful candidates will be subject to an Enhanced DBS/PVG check and Regulated Activity which will include a check against the Barred adult list. * Some of our roles require male or female employees only, where this is indicated it is a genuine occupational requirement, in accordance with the Equality Act 2010 Role Specific Requirements - Driver: Driver Required Gender: No Specific Requirement
Store Supervisor applicants will be reliable with a professional and focused approach to store operations, leadership and development, taking direction from and supporting the Store and Store Assistant Managers in day-to-day operations. The appointed Store Supervisor will be required to complete the Home Bargains Management Training Programme as part of their ongoing development...... click apply for full job details
Dec 01, 2020
Full time
Store Supervisor applicants will be reliable with a professional and focused approach to store operations, leadership and development, taking direction from and supporting the Store and Store Assistant Managers in day-to-day operations. The appointed Store Supervisor will be required to complete the Home Bargains Management Training Programme as part of their ongoing development...... click apply for full job details
Key Education are currently supporting an outstanding school in North West Cambridgeshire who are looking for a Design Technology & Engineering teacher to start ASAP. This will be on a full time, fixed term contract directly with the school which will be required until Easter 2021. You will be teaching Design Technology & Engineering to KS3 and KS4. (There is scope to teach just DT.) Ideally you will hold QTS/QTLS. NQT's are welcome to apply and this would be a brilliant opportunity to complete a term of your induction in a forward-thinking school. Key Education is an independent agency who has serviced education establishments across the East of England for over 14 years. We work hard to stand out from the crowd and go the extra mile to provide a personable service to our teachers, taking on board your circumstances and working with you to find the right position. If you are interested in being considered for this position, please apply with an up to date CV. You will be required to complete our registration form and registration will be subject to references and an enhanced DBS that is registered with the Update Service.
Dec 01, 2020
Full time
Key Education are currently supporting an outstanding school in North West Cambridgeshire who are looking for a Design Technology & Engineering teacher to start ASAP. This will be on a full time, fixed term contract directly with the school which will be required until Easter 2021. You will be teaching Design Technology & Engineering to KS3 and KS4. (There is scope to teach just DT.) Ideally you will hold QTS/QTLS. NQT's are welcome to apply and this would be a brilliant opportunity to complete a term of your induction in a forward-thinking school. Key Education is an independent agency who has serviced education establishments across the East of England for over 14 years. We work hard to stand out from the crowd and go the extra mile to provide a personable service to our teachers, taking on board your circumstances and working with you to find the right position. If you are interested in being considered for this position, please apply with an up to date CV. You will be required to complete our registration form and registration will be subject to references and an enhanced DBS that is registered with the Update Service.
