Help us change lives At Exact Sciences, we're helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you're working to help others. Company Overview Exact Sciences is dedicated to delivering patient critical answers across the cancer journey from early detection to treatment decision making. With a strong focus on people and an empathetic spirit, which fuels the company's culture, driving them to create and deliver solutions rooted in the needs of patients, providers, and families. From earlier cancer detection to treatment guidance and monitoring, Exact Sciences are helping people get the answers they need to make more informed decisions across the cancer continuum. With a leading portfolio of products for earlier detection and treatment guidance, they help people face the most challenging decisions with confidence with a dedication to continuously innovate, combining scientific rigor with an open-minded approach to deliver the next big thing. Exact Sciences is continuously expanding the pipeline with the aim of tackling a wider array of cancer tests through the following measures: Expanding the Oncotype IQ platform to include liquid and tissue-based tests, all with the goal of making cancer care smarter. Adapting biomarker-based technologies create a liquid biopsy capable of detecting cancers and precancers from a blood sample. Using their proven multi-marker approach to achieve analytical sensitivity needed to discriminate between normal and cancerous samples. Collaborating with world-class clinicians and scientists at Mayo Clinic to identify biomarkers associated with the 15 deadliest cancers. Building a cancer detection platform upon learnings from the development of Cologuard (commercially available in the US only). By 2020, Oncotype DX will have been used to guide treatment decisions for more than 1 million cancer patients worldwide in breast, prostate and colon cancer. In July 2019 Exact Sciences acquired Genomic Health, a genetic cancer detection company based in Redwood City, California, for USD 2.8 billion, creating the leading global cancer diagnostics company. In 2020 Exact Sciences acquired Thrive Earlier Detection Corp., a Massachusetts-based healthcare company, in a multi-billion-dollar deal, and Base Genomics, which has technology for DNA methylation analysis. In February 2021 Exact Sciences announced the acquisition of Ashion Analytics, LLC (Ashion) from The Translational Genomics Research Institute (TGen), an affiliate of City of Hope. Ashion is a CLIA-certified and CAP-accredited sequencing lab based in Phoenix, Arizona with the genomics testing capabilities necessary to address the increasingly complex needs of clinical, academic, and biopharma customers focused on precision cancer treatments. The company is based in the United States, with International headquarters in Zug, Switzerland. Position Summary The Medical Affairs Senior Manager, MSL & Expansion Markets, France is a hybrid role responsible for leading an international team of Medical Science Liaisons and supporting Exact Sciences International expansion strategy with key medical activities. This is an exciting chance to build the first Exact Sciences International MSL team in leading and executing an efficient and transparent conversion plan to bring MSL contractors in-house as well as hire and onboard new MSLs to create a diverse and inclusive team. The International Medical Affairs Senior Manager - MSL & Expansion Markets will be expected to develop and drive MSL strategy ensure field medical activities and insight generation result in demonstrable outcomes and further develop and grow the MSL capability at Exact Sciences International. In addition, this individual will be responsible for medical affairs activities in selected key markets across International. These markets will include those where we want to move directly into a market (currently through distributors) or those markets where we currently have limited patient access that require improved reimbursement pathways. The Medical lead will work closely with the Market Expansion Team and lead all associated medial activities that may include leading medical activities for change in market reimbursement, aligning new market needs with central medical team, developing core data strategy for new markets, and defining resourcing needs and transition to new hires. The position is also responsible for consolidating and interpreting medical intelligence and reporting it to the Expansion Markets team. The incumbent will work closely with other functions within the company, including Corporate Strategy, Marketing, and Commercial to advance cross-functional understanding of the MSL value proposition, identify gaps and achieve results in line with company objectives. Representing the medical function, this individual will also manage research and educational medical objectives, while supporting commercial business and reimbursement objectives for the Oncotype DX breast recurrence score test. This position requires professionals with established personal and scientific creditability to interact with thought leaders, government health authorities, and medical centers of excellence. This is a dynamic role and will continue to evolve. Responsibilities/Duties Lead an international team of MSLs toward the implementation of field medical activities by communicating expectations and guiding the team to maintain and effectively communicate deep scientific knowledge and excel at KOL engagement and support medical/scientific information needs of scientific and clinical experts. Accompany the team to meetings with KOLs and other HCPs to assess proficiency and provide timely and constructive performance feedback. Lead and coordinate MSL team meetings to support team building, best practice sharing, development, and the accomplishment of field medical objectives. Develop a MSL Strategic Plan as well as Medical Plan for the markets, which include plans for KOL engagement, data generation, educational and guideline initiatives and reimbursement initiatives that align with the business objectives. Identify and engage international, national, and regional thought leaders in breast cancer within assigned geographic regions to conduct scientific discussions and understand insights related to molecular diagnostics in early BC management, while also establishing and maintaining professional relationships with them. Act as primary contact for investigators interested in developing and performing studies with the company's commercially available assays in breast cancer. Assist in R&D and investigator-initiated studies as appropriate. Lead national and regional Advisory Boards when external advice is needed. Provide clinical presentations and information in academic, community, and healthcare provider setting in both group and one-on-one situations. Support & partner with regional team to deliver key medical activities. Developing medical slides, giving medical training presentations, and training in internal meetings and for partner distributors. Support international access & reimbursement with medical and scientific expertise. Assure compliance with relevant corporate policies. Provide feedback and medical input to local commercial plans and strategies. Pivotal Experience & Expertise Degree in Medicine/Medical Doctor or PhD, PharmD. 3+ years of therapeutic clinical experience desired. 5 to 7 years of industry experience (working in pharma/biotech/med tech). At least 3 years in a Medical Science Liaison role. Previous MSL (or other) management experience. Expertise in Oncology. Experience in breast/GI/lung cancer is a plus. Experience in Diagnostics or Biotech industry is a plus. Experience in relevant geographies a plus. Excellent English. Skills in other languages preferred. Excellent oral, written and presentation communication skills. Ability to independently deliver quality results in a timely manner. Proven record of working in matrix environment and delivering as part of a cross-functional team. Track record of delivering innovative medical activities across markets. Cultural Impact Highest integrity and ethical behavior. Mutual respect for colleagues. Collaborative within teams, uses resources carefully and can build a great place to work and grow. Ability to interact within culturally diverse teams. Business acumen and innovative mindset. Ability to manage though complexity and ambiguity, while focusing on the end goal. Other Office-based in the International headquarters in Zug or out of one of our European offices. Ability to travel approx >50%. Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, email . We'll work with you to meet your accessibility needs. Not ready to apply? Join our talent community and stay up to date on what's new at Exact Sciences.
Apr 18, 2024
Full time
Help us change lives At Exact Sciences, we're helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you're working to help others. Company Overview Exact Sciences is dedicated to delivering patient critical answers across the cancer journey from early detection to treatment decision making. With a strong focus on people and an empathetic spirit, which fuels the company's culture, driving them to create and deliver solutions rooted in the needs of patients, providers, and families. From earlier cancer detection to treatment guidance and monitoring, Exact Sciences are helping people get the answers they need to make more informed decisions across the cancer continuum. With a leading portfolio of products for earlier detection and treatment guidance, they help people face the most challenging decisions with confidence with a dedication to continuously innovate, combining scientific rigor with an open-minded approach to deliver the next big thing. Exact Sciences is continuously expanding the pipeline with the aim of tackling a wider array of cancer tests through the following measures: Expanding the Oncotype IQ platform to include liquid and tissue-based tests, all with the goal of making cancer care smarter. Adapting biomarker-based technologies create a liquid biopsy capable of detecting cancers and precancers from a blood sample. Using their proven multi-marker approach to achieve analytical sensitivity needed to discriminate between normal and cancerous samples. Collaborating with world-class clinicians and scientists at Mayo Clinic to identify biomarkers associated with the 15 deadliest cancers. Building a cancer detection platform upon learnings from the development of Cologuard (commercially available in the US only). By 2020, Oncotype DX will have been used to guide treatment decisions for more than 1 million cancer patients worldwide in breast, prostate and colon cancer. In July 2019 Exact Sciences acquired Genomic Health, a genetic cancer detection company based in Redwood City, California, for USD 2.8 billion, creating the leading global cancer diagnostics company. In 2020 Exact Sciences acquired Thrive Earlier Detection Corp., a Massachusetts-based healthcare company, in a multi-billion-dollar deal, and Base Genomics, which has technology for DNA methylation analysis. In February 2021 Exact Sciences announced the acquisition of Ashion Analytics, LLC (Ashion) from The Translational Genomics Research Institute (TGen), an affiliate of City of Hope. Ashion is a CLIA-certified and CAP-accredited sequencing lab based in Phoenix, Arizona with the genomics testing capabilities necessary to address the increasingly complex needs of clinical, academic, and biopharma customers focused on precision cancer treatments. The company is based in the United States, with International headquarters in Zug, Switzerland. Position Summary The Medical Affairs Senior Manager, MSL & Expansion Markets, France is a hybrid role responsible for leading an international team of Medical Science Liaisons and supporting Exact Sciences International expansion strategy with key medical activities. This is an exciting chance to build the first Exact Sciences International MSL team in leading and executing an efficient and transparent conversion plan to bring MSL contractors in-house as well as hire and onboard new MSLs to create a diverse and inclusive team. The International Medical Affairs Senior Manager - MSL & Expansion Markets will be expected to develop and drive MSL strategy ensure field medical activities and insight generation result in demonstrable outcomes and further develop and grow the MSL capability at Exact Sciences International. In addition, this individual will be responsible for medical affairs activities in selected key markets across International. These markets will include those where we want to move directly into a market (currently through distributors) or those markets where we currently have limited patient access that require improved reimbursement pathways. The Medical lead will work closely with the Market Expansion Team and lead all associated medial activities that may include leading medical activities for change in market reimbursement, aligning new market needs with central medical team, developing core data strategy for new markets, and defining resourcing needs and transition to new hires. The position is also responsible for consolidating and interpreting medical intelligence and reporting it to the Expansion Markets team. The incumbent will work closely with other functions within the company, including Corporate Strategy, Marketing, and Commercial to advance cross-functional understanding of the MSL value proposition, identify gaps and achieve results in line with company objectives. Representing the medical function, this individual will also manage research and educational medical objectives, while supporting commercial business and reimbursement objectives for the Oncotype DX breast recurrence score test. This position requires professionals with established personal and scientific creditability to interact with thought leaders, government health authorities, and medical centers of excellence. This is a dynamic role and will continue to evolve. Responsibilities/Duties Lead an international team of MSLs toward the implementation of field medical activities by communicating expectations and guiding the team to maintain and effectively communicate deep scientific knowledge and excel at KOL engagement and support medical/scientific information needs of scientific and clinical experts. Accompany the team to meetings with KOLs and other HCPs to assess proficiency and provide timely and constructive performance feedback. Lead and coordinate MSL team meetings to support team building, best practice sharing, development, and the accomplishment of field medical objectives. Develop a MSL Strategic Plan as well as Medical Plan for the markets, which include plans for KOL engagement, data generation, educational and guideline initiatives and reimbursement initiatives that align with the business objectives. Identify and engage international, national, and regional thought leaders in breast cancer within assigned geographic regions to conduct scientific discussions and understand insights related to molecular diagnostics in early BC management, while also establishing and maintaining professional relationships with them. Act as primary contact for investigators interested in developing and performing studies with the company's commercially available assays in breast cancer. Assist in R&D and investigator-initiated studies as appropriate. Lead national and regional Advisory Boards when external advice is needed. Provide clinical presentations and information in academic, community, and healthcare provider setting in both group and one-on-one situations. Support & partner with regional team to deliver key medical activities. Developing medical slides, giving medical training presentations, and training in internal meetings and for partner distributors. Support international access & reimbursement with medical and scientific expertise. Assure compliance with relevant corporate policies. Provide feedback and medical input to local commercial plans and strategies. Pivotal Experience & Expertise Degree in Medicine/Medical Doctor or PhD, PharmD. 3+ years of therapeutic clinical experience desired. 5 to 7 years of industry experience (working in pharma/biotech/med tech). At least 3 years in a Medical Science Liaison role. Previous MSL (or other) management experience. Expertise in Oncology. Experience in breast/GI/lung cancer is a plus. Experience in Diagnostics or Biotech industry is a plus. Experience in relevant geographies a plus. Excellent English. Skills in other languages preferred. Excellent oral, written and presentation communication skills. Ability to independently deliver quality results in a timely manner. Proven record of working in matrix environment and delivering as part of a cross-functional team. Track record of delivering innovative medical activities across markets. Cultural Impact Highest integrity and ethical behavior. Mutual respect for colleagues. Collaborative within teams, uses resources carefully and can build a great place to work and grow. Ability to interact within culturally diverse teams. Business acumen and innovative mindset. Ability to manage though complexity and ambiguity, while focusing on the end goal. Other Office-based in the International headquarters in Zug or out of one of our European offices. Ability to travel approx >50%. Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, email . We'll work with you to meet your accessibility needs. Not ready to apply? Join our talent community and stay up to date on what's new at Exact Sciences.
Consulting Director - Environment, Climate Policy Evaluation page is loaded Consulting Director - Environment, Climate Policy Evaluation Apply locations London (GB80) time type Full time posted on Posted 2 Days Ago job requisition id R At ICF, your evaluation and research skills deliver a real-world impact. Over the past two decades, we've become the leading provider of evaluation services to the UK's Department for Environment, Food & Rural Affairs (Defra), as well as Natural England, the Environment Agency and other government agencies. We're now looking for an experienced evaluation service leader to join our talented team of experts in environmental and resource policies. This is your opportunity to shape the future of UK environmental policy, to see it in action, and to evaluate the difference it makes in the real world. The Monitoring and Evaluation (MEL) frameworks we have with Defra, and our established role on its Research and Development and Evidence framework, offer access to a range of secure, long-term opportunities that are unmatched in the sector. Why ICF? ICF's experts are thought leaders across a huge range of disciplines. Our approach is always collegiate and personal. You'll join a team that's focused only on delivering positive impact. Respect for new ideas and expertise means we're always ready to embrace differences. We're never afraid to ask if there is a better way to do something. This role offers you the chance to develop your career within a global business that takes a collaborative approach to working with our unrivalled network of experts here in the UK. We are looking for an experienced evaluation leader with expertise of applying evaluation methods in one more or the following policy areas, preferably in a UK context: Air quality Water quality Pollution Water resources Waste and resources Flood and coastal erosion risk management Climate change, climate adaptation and Net Zero Land use and land access. In your new role you will: Design and direct a portfolio of evaluation studies on government policies relating to the topics listed above. Contribute to the development and delivery of our wider evaluation service offer for the Defra family, working with our senior leadership. Provide technical, management and development support to colleagues who are at an earlier stage of career progression. You will come to us with: A strong track record in the design and delivery of environmental policy evaluations, research and analysis for the UK Government, working as a project director and service leader. An expert understanding of the theory and application of impact and/or process evaluation methods in accordance with Magenta Book guidance. Experience of leadership in a consulting or similar project-based environment. Strong project management and commercial skills and expertise in business or major programme leadership. Excellent written and verbal communication skills. This role will be positioned as a Consulting Director or Lead Managing Consultant level depending on experience. About us: Working at ICF means applying a passion for meaningful work with intellectual rigor to help solve the leading issues of our day. Smart, compassionate, innovative, committed, ICF employees tackle unprecedented challenges to benefit people, businesses, and governments around the globe. We believe in collaboration, mutual respect, open communication, and opportunity for growth. We can only solve the world's toughest challenges by building an inclusive workplace that allows everyone to thrive. We are committed to creating a culture where we embrace our differences in ideas and identities. Together, our employees are empowered to share their expertise and collaborate with others to achieve personal and professional goals. Learn more about what we do and our commitment to inclusion . The benefits of joining ICF: Our people at ICF are our most important asset, so we invest in them from the moment they arrive. When you join our team, you'll have access to a vast array of benefits to help you live your life well. We offer a hybrid working policy, which will provide you with the flexibility to collaborate in the office, as well as in the comfort of your own home, ensuring you are able to successfully deliver the requirements of your role. To support you, our employee wellbeing hub is designed to provide highly personalised support across a comprehensive range of wellbeing issues, such as mind, body, finances, community, career programs and HR support. We enjoy celebrating success, which is why we have a competitive recognition program called 'You Matter', which awards points as a 'thank you' for your work achievements. These can be spent on a large variety of high-quality items, as well as online or high-street vouchers, all with zero tax payable by the employee. ICF also offers a range of competitive benefits, which include: Single Private Medical Insurance cover with no restrictions on existing conditions. Dental insurance and an online GP service. 25 days annual leave, plus UK bank holidays (annual leave increases with years of service). Pension scheme with 5% of salary employer contribution Life assurance paying 4x annual salary and Group Income Protection paying 66% of salary for up to 5 years if you are off work on long-term sick. Enhanced parental leave policies, enhanced maternity, paternity, adoption, and shared parental pay. London (GB80) Similar Jobs (2) Consulting Director: Farming, food and environment policy evaluation locations 4 Locations time type Full time posted on Posted 2 Days Ago Principal Environmental Data Specialist locations 4 Locations time type Full time posted on Posted 3 Days Ago ICF is a global consulting and technology services company with approximately 9,000 employees, but we are not your typical consultants. At ICF, business analysts and policy specialists work together with digital strategists, data scientists and creatives. We combine unmatched industry expertise with cutting-edge engagement capabilities to help organizations solve their most complex challenges. Since 1969, public and private sector clients have worked with ICF to navigate change and shape the future. Learn more at .
Apr 16, 2024
Full time
Consulting Director - Environment, Climate Policy Evaluation page is loaded Consulting Director - Environment, Climate Policy Evaluation Apply locations London (GB80) time type Full time posted on Posted 2 Days Ago job requisition id R At ICF, your evaluation and research skills deliver a real-world impact. Over the past two decades, we've become the leading provider of evaluation services to the UK's Department for Environment, Food & Rural Affairs (Defra), as well as Natural England, the Environment Agency and other government agencies. We're now looking for an experienced evaluation service leader to join our talented team of experts in environmental and resource policies. This is your opportunity to shape the future of UK environmental policy, to see it in action, and to evaluate the difference it makes in the real world. The Monitoring and Evaluation (MEL) frameworks we have with Defra, and our established role on its Research and Development and Evidence framework, offer access to a range of secure, long-term opportunities that are unmatched in the sector. Why ICF? ICF's experts are thought leaders across a huge range of disciplines. Our approach is always collegiate and personal. You'll join a team that's focused only on delivering positive impact. Respect for new ideas and expertise means we're always ready to embrace differences. We're never afraid to ask if there is a better way to do something. This role offers you the chance to develop your career within a global business that takes a collaborative approach to working with our unrivalled network of experts here in the UK. We are looking for an experienced evaluation leader with expertise of applying evaluation methods in one more or the following policy areas, preferably in a UK context: Air quality Water quality Pollution Water resources Waste and resources Flood and coastal erosion risk management Climate change, climate adaptation and Net Zero Land use and land access. In your new role you will: Design and direct a portfolio of evaluation studies on government policies relating to the topics listed above. Contribute to the development and delivery of our wider evaluation service offer for the Defra family, working with our senior leadership. Provide technical, management and development support to colleagues who are at an earlier stage of career progression. You will come to us with: A strong track record in the design and delivery of environmental policy evaluations, research and analysis for the UK Government, working as a project director and service leader. An expert understanding of the theory and application of impact and/or process evaluation methods in accordance with Magenta Book guidance. Experience of leadership in a consulting or similar project-based environment. Strong project management and commercial skills and expertise in business or major programme leadership. Excellent written and verbal communication skills. This role will be positioned as a Consulting Director or Lead Managing Consultant level depending on experience. About us: Working at ICF means applying a passion for meaningful work with intellectual rigor to help solve the leading issues of our day. Smart, compassionate, innovative, committed, ICF employees tackle unprecedented challenges to benefit people, businesses, and governments around the globe. We believe in collaboration, mutual respect, open communication, and opportunity for growth. We can only solve the world's toughest challenges by building an inclusive workplace that allows everyone to thrive. We are committed to creating a culture where we embrace our differences in ideas and identities. Together, our employees are empowered to share their expertise and collaborate with others to achieve personal and professional goals. Learn more about what we do and our commitment to inclusion . The benefits of joining ICF: Our people at ICF are our most important asset, so we invest in them from the moment they arrive. When you join our team, you'll have access to a vast array of benefits to help you live your life well. We offer a hybrid working policy, which will provide you with the flexibility to collaborate in the office, as well as in the comfort of your own home, ensuring you are able to successfully deliver the requirements of your role. To support you, our employee wellbeing hub is designed to provide highly personalised support across a comprehensive range of wellbeing issues, such as mind, body, finances, community, career programs and HR support. We enjoy celebrating success, which is why we have a competitive recognition program called 'You Matter', which awards points as a 'thank you' for your work achievements. These can be spent on a large variety of high-quality items, as well as online or high-street vouchers, all with zero tax payable by the employee. ICF also offers a range of competitive benefits, which include: Single Private Medical Insurance cover with no restrictions on existing conditions. Dental insurance and an online GP service. 25 days annual leave, plus UK bank holidays (annual leave increases with years of service). Pension scheme with 5% of salary employer contribution Life assurance paying 4x annual salary and Group Income Protection paying 66% of salary for up to 5 years if you are off work on long-term sick. Enhanced parental leave policies, enhanced maternity, paternity, adoption, and shared parental pay. London (GB80) Similar Jobs (2) Consulting Director: Farming, food and environment policy evaluation locations 4 Locations time type Full time posted on Posted 2 Days Ago Principal Environmental Data Specialist locations 4 Locations time type Full time posted on Posted 3 Days Ago ICF is a global consulting and technology services company with approximately 9,000 employees, but we are not your typical consultants. At ICF, business analysts and policy specialists work together with digital strategists, data scientists and creatives. We combine unmatched industry expertise with cutting-edge engagement capabilities to help organizations solve their most complex challenges. Since 1969, public and private sector clients have worked with ICF to navigate change and shape the future. Learn more at .
Newton Colmore Consulting Ltd
Cambridge, Cambridgeshire
Post-Doc Chemist - Battery Technology - Cambridge A rapidly growing scientific technology house based in Cambridge are in the process of expansion and are actively looking to strengthen their in-house research team by bringing on a Post-Doc Chemist to work on battery technologies. As a Post-Doc Chemist, you will be charged with developing the company's next generation energy storage materials. This will include working within a multidisciplinary team or scientist and engineers to maximise the performance of battery materials and contribute to developing a deep understanding of the key structure - property relationships in functional battery materials and materials formulations. Some other key parts to the role will include; Formulation of functional material inks and pastes and their pre-device fabrication physical characterisation. Creative contributions to brainstorms, studies, and project meeting discussions. Proposal and design of novel materials and recommendations to solve chemical synthetic issues. To be considered for this role we are looking for people with strong knowledge of synthetic organic chemistry and polymers that complements a PhD in Chemistry. Any experience with battery technologies or electrochemical techniques would be a significant advantage. In return for your hard work the company offer a highly competitive salary and benefits package as well providing excellent career progression opportunities and the chance to work on leading edge technologies. This is a 2 year fixed term contract with possibilities for future roles in within the organisation. For more information contact Matthew Lowdon of Newton Colmore Consulting on . To enter the recruitment process click apply now and if you have the right skills and expertise I will be in touch to discuss the opportunity further. Newton Colmore Consulting is a highly specialist recruitment consultancy operating within the medical devices, Scientific Engineering, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors throughout Europe and the US. Keywords: Senior Chemist, Energy Storage Systems, Synthetic Chemistry, OLED, Materials Engineering, organometallic.
Feb 22, 2022
Full time
Post-Doc Chemist - Battery Technology - Cambridge A rapidly growing scientific technology house based in Cambridge are in the process of expansion and are actively looking to strengthen their in-house research team by bringing on a Post-Doc Chemist to work on battery technologies. As a Post-Doc Chemist, you will be charged with developing the company's next generation energy storage materials. This will include working within a multidisciplinary team or scientist and engineers to maximise the performance of battery materials and contribute to developing a deep understanding of the key structure - property relationships in functional battery materials and materials formulations. Some other key parts to the role will include; Formulation of functional material inks and pastes and their pre-device fabrication physical characterisation. Creative contributions to brainstorms, studies, and project meeting discussions. Proposal and design of novel materials and recommendations to solve chemical synthetic issues. To be considered for this role we are looking for people with strong knowledge of synthetic organic chemistry and polymers that complements a PhD in Chemistry. Any experience with battery technologies or electrochemical techniques would be a significant advantage. In return for your hard work the company offer a highly competitive salary and benefits package as well providing excellent career progression opportunities and the chance to work on leading edge technologies. This is a 2 year fixed term contract with possibilities for future roles in within the organisation. For more information contact Matthew Lowdon of Newton Colmore Consulting on . To enter the recruitment process click apply now and if you have the right skills and expertise I will be in touch to discuss the opportunity further. Newton Colmore Consulting is a highly specialist recruitment consultancy operating within the medical devices, Scientific Engineering, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors throughout Europe and the US. Keywords: Senior Chemist, Energy Storage Systems, Synthetic Chemistry, OLED, Materials Engineering, organometallic.
I am collaborating with a top-10 global drug development company who manage the entire life cycle of the drug development process primarily within Oncology/Haematology. With >250 clinical trials completed within the last 5 years in these therapeutic areas, my client is a world leader in oncology and haematology drug development. We are seeking a physician with a strong research background in Oncology/Haematology. *Key responsibilities* * Provide medical expertise at the global level across the entire scope of the drug development process * Develop and deliver expert training programs * Represent the clinical development team within Legal, Medical affairs and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients and Key Opinion Leaders (KOLs) * Collaborating with Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Oversee strategic clinical trial progression across a variety of tumour sub-types and therapy areas. * Autonomy within a cross-functional collaborative team environment *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Oncology, Haematology, Paediatrics' or Internal medicine required * Investigator experience in Oncology or Onco-Haematology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Comprehensive salary * Enhanced bonus scheme * Company Car * Market leading Pension Scheme * Private Health Insurance * Relocation package * Travel allowance * 30+ days holiday * Clear development pathway *Get in touch...* * Contact: Francesca Hallworth * Clinical Development and Medical Affairs Recruitment Consultant * Email: [fhallworth barringtonjames.com](mailto:)
Dec 08, 2021
Full time
I am collaborating with a top-10 global drug development company who manage the entire life cycle of the drug development process primarily within Oncology/Haematology. With >250 clinical trials completed within the last 5 years in these therapeutic areas, my client is a world leader in oncology and haematology drug development. We are seeking a physician with a strong research background in Oncology/Haematology. *Key responsibilities* * Provide medical expertise at the global level across the entire scope of the drug development process * Develop and deliver expert training programs * Represent the clinical development team within Legal, Medical affairs and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients and Key Opinion Leaders (KOLs) * Collaborating with Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Oversee strategic clinical trial progression across a variety of tumour sub-types and therapy areas. * Autonomy within a cross-functional collaborative team environment *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Oncology, Haematology, Paediatrics' or Internal medicine required * Investigator experience in Oncology or Onco-Haematology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Comprehensive salary * Enhanced bonus scheme * Company Car * Market leading Pension Scheme * Private Health Insurance * Relocation package * Travel allowance * 30+ days holiday * Clear development pathway *Get in touch...* * Contact: Francesca Hallworth * Clinical Development and Medical Affairs Recruitment Consultant * Email: [fhallworth barringtonjames.com](mailto:)
I am collaborating with a top-10 global drug development company who manage the entire life cycle of the drug development process primarily within Oncology/Haematology. With >250 clinical trials completed within the last 5 years in these therapeutic areas, my client is a world leader in oncology and haematology drug development. We are seeking a physician with a strong research background in Oncology/Haematology. *Key responsibilities* * Provide medical expertise at the global level across the entire scope of the drug development process * Develop and deliver expert training programs * Represent the clinical development team within Legal, Medical affairs and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients and Key Opinion Leaders (KOLs) * Collaborating with Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Oversee strategic clinical trial progression across a variety of tumour sub-types and therapy areas. * Autonomy within a cross-functional collaborative team environment *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Oncology, Haematology, Paediatrics' or Internal medicine required * Investigator experience in Oncology or Onco-Haematology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Comprehensive salary * Enhanced bonus scheme * Company Car * Market leading Pension Scheme * Private Health Insurance * Relocation package * Travel allowance * 30+ days holiday * Clear development pathway *Get in touch...* * Contact: Francesca Hallworth * Clinical Development and Medical Affairs Recruitment Consultant * Email: [fhallworth barringtonjames.com](mailto:)
Dec 08, 2021
Full time
I am collaborating with a top-10 global drug development company who manage the entire life cycle of the drug development process primarily within Oncology/Haematology. With >250 clinical trials completed within the last 5 years in these therapeutic areas, my client is a world leader in oncology and haematology drug development. We are seeking a physician with a strong research background in Oncology/Haematology. *Key responsibilities* * Provide medical expertise at the global level across the entire scope of the drug development process * Develop and deliver expert training programs * Represent the clinical development team within Legal, Medical affairs and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients and Key Opinion Leaders (KOLs) * Collaborating with Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Oversee strategic clinical trial progression across a variety of tumour sub-types and therapy areas. * Autonomy within a cross-functional collaborative team environment *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Oncology, Haematology, Paediatrics' or Internal medicine required * Investigator experience in Oncology or Onco-Haematology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Comprehensive salary * Enhanced bonus scheme * Company Car * Market leading Pension Scheme * Private Health Insurance * Relocation package * Travel allowance * 30+ days holiday * Clear development pathway *Get in touch...* * Contact: Francesca Hallworth * Clinical Development and Medical Affairs Recruitment Consultant * Email: [fhallworth barringtonjames.com](mailto:)
Do you want to drive the development and commercialization of medicines that will provide treatment to patients with little or no alternate options? My client manages the entire life cycle of the drug development process, we are looking to expand within Rheumatology. With >250 clinical trials completed within the last 5 years, my client is a world leader in developing clinical trials and bringing new therapeutics to the market. If you have a clinical background in Rheumatology and experience as an investigator or experience working with clinical trials in the pharmaceutical/Biotech/CRO industry, I welcome you to read below: *Key responsibilities* * Provide medical expertise across the entire scope of clinical development and medical affairs * Develop and deliver expert training programs * Represent Medical Affairs within Legal, Medical and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients * Collaborating with our Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Ownership and oversight of strategic clinical trial progression across a variety of tumour sub-types and therapy areas. *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Rheumatology * Investigator experience in Rheumatology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Highly competitive basic salary * Company Car * Private Healthcare * Excellent bonus scheme * Senior role within a top-5 Global Health Science Company * Clear internal promotion pathway * Flexibility in terms of office location * Opportunity to travel the world * Spearhead the development of novel therapeutics *Get in touch...* * Contact: Vincenzo B. Dessena BSc. MSc. * Clinical Development and Medical Affairs Recruitment Consultant * Email: [vdessena (at) barringtonjames.com](mailto:)
Sep 15, 2021
Full time
Do you want to drive the development and commercialization of medicines that will provide treatment to patients with little or no alternate options? My client manages the entire life cycle of the drug development process, we are looking to expand within Rheumatology. With >250 clinical trials completed within the last 5 years, my client is a world leader in developing clinical trials and bringing new therapeutics to the market. If you have a clinical background in Rheumatology and experience as an investigator or experience working with clinical trials in the pharmaceutical/Biotech/CRO industry, I welcome you to read below: *Key responsibilities* * Provide medical expertise across the entire scope of clinical development and medical affairs * Develop and deliver expert training programs * Represent Medical Affairs within Legal, Medical and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients * Collaborating with our Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Ownership and oversight of strategic clinical trial progression across a variety of tumour sub-types and therapy areas. *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Rheumatology * Investigator experience in Rheumatology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Highly competitive basic salary * Company Car * Private Healthcare * Excellent bonus scheme * Senior role within a top-5 Global Health Science Company * Clear internal promotion pathway * Flexibility in terms of office location * Opportunity to travel the world * Spearhead the development of novel therapeutics *Get in touch...* * Contact: Vincenzo B. Dessena BSc. MSc. * Clinical Development and Medical Affairs Recruitment Consultant * Email: [vdessena (at) barringtonjames.com](mailto:)
Do you want to drive the development and commercialization of medicines that will provide treatment to patients with little or no alternate options? My client manages the entire life cycle of the drug development process, we are looking to expand within Rheumatology. With >250 clinical trials completed within the last 5 years, my client is a world leader in developing clinical trials and bringing new therapeutics to the market. If you have a clinical background in Rheumatology and experience as an investigator or experience working with clinical trials in the pharmaceutical/Biotech/CRO industry, I welcome you to read below: *Key responsibilities* * Provide medical expertise across the entire scope of clinical development and medical affairs * Develop and deliver expert training programs * Represent Medical Affairs within Legal, Medical and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients * Collaborating with our Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Ownership and oversight of strategic clinical trial progression across a variety of tumour sub-types and therapy areas. *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Rheumatology * Investigator experience in Rheumatology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Highly competitive basic salary * Company Car * Private Healthcare * Excellent bonus scheme * Senior role within a top-5 Global Health Science Company * Clear internal promotion pathway * Flexibility in terms of office location * Opportunity to travel the world * Spearhead the development of novel therapeutics *Get in touch...* * Contact: Vincenzo B. Dessena BSc. MSc. * Clinical Development and Medical Affairs Recruitment Consultant * Email: [vdessena (at) barringtonjames.com](mailto:)
Sep 15, 2021
Full time
Do you want to drive the development and commercialization of medicines that will provide treatment to patients with little or no alternate options? My client manages the entire life cycle of the drug development process, we are looking to expand within Rheumatology. With >250 clinical trials completed within the last 5 years, my client is a world leader in developing clinical trials and bringing new therapeutics to the market. If you have a clinical background in Rheumatology and experience as an investigator or experience working with clinical trials in the pharmaceutical/Biotech/CRO industry, I welcome you to read below: *Key responsibilities* * Provide medical expertise across the entire scope of clinical development and medical affairs * Develop and deliver expert training programs * Represent Medical Affairs within Legal, Medical and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients * Collaborating with our Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Ownership and oversight of strategic clinical trial progression across a variety of tumour sub-types and therapy areas. *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Rheumatology * Investigator experience in Rheumatology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Highly competitive basic salary * Company Car * Private Healthcare * Excellent bonus scheme * Senior role within a top-5 Global Health Science Company * Clear internal promotion pathway * Flexibility in terms of office location * Opportunity to travel the world * Spearhead the development of novel therapeutics *Get in touch...* * Contact: Vincenzo B. Dessena BSc. MSc. * Clinical Development and Medical Affairs Recruitment Consultant * Email: [vdessena (at) barringtonjames.com](mailto:)
Do you want to drive the development and commercialization of medicines that will provide treatment to patients with little or no alternate options? My client manages the entire life cycle of the drug development process, we are looking to expand within Rheumatology. With >250 clinical trials completed within the last 5 years, my client is a world leader in developing clinical trials and bringing new therapeutics to the market. If you have a clinical background in Rheumatology and experience as an investigator or experience working with clinical trials in the pharmaceutical/Biotech/CRO industry, I welcome you to read below: *Key responsibilities* * Provide medical expertise across the entire scope of clinical development and medical affairs * Develop and deliver expert training programs * Represent Medical Affairs within Legal, Medical and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients * Collaborating with our Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Ownership and oversight of strategic clinical trial progression across a variety of tumour sub-types and therapy areas. *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Rheumatology * Investigator experience in Rheumatology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Highly competitive basic salary * Company Car * Private Healthcare * Excellent bonus scheme * Senior role within a top-5 Global Health Science Company * Clear internal promotion pathway * Flexibility in terms of office location * Opportunity to travel the world * Spearhead the development of novel therapeutics *Get in touch...* * Contact: Vincenzo B. Dessena BSc. MSc. * Clinical Development and Medical Affairs Recruitment Consultant * Email: [vdessena (at) barringtonjames.com](mailto:)
Sep 15, 2021
Full time
Do you want to drive the development and commercialization of medicines that will provide treatment to patients with little or no alternate options? My client manages the entire life cycle of the drug development process, we are looking to expand within Rheumatology. With >250 clinical trials completed within the last 5 years, my client is a world leader in developing clinical trials and bringing new therapeutics to the market. If you have a clinical background in Rheumatology and experience as an investigator or experience working with clinical trials in the pharmaceutical/Biotech/CRO industry, I welcome you to read below: *Key responsibilities* * Provide medical expertise across the entire scope of clinical development and medical affairs * Develop and deliver expert training programs * Represent Medical Affairs within Legal, Medical and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients * Collaborating with our Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Ownership and oversight of strategic clinical trial progression across a variety of tumour sub-types and therapy areas. *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Rheumatology * Investigator experience in Rheumatology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Highly competitive basic salary * Company Car * Private Healthcare * Excellent bonus scheme * Senior role within a top-5 Global Health Science Company * Clear internal promotion pathway * Flexibility in terms of office location * Opportunity to travel the world * Spearhead the development of novel therapeutics *Get in touch...* * Contact: Vincenzo B. Dessena BSc. MSc. * Clinical Development and Medical Affairs Recruitment Consultant * Email: [vdessena (at) barringtonjames.com](mailto:)
Do you want to drive the development and commercialization of medicines that will provide treatment to patients with little or no alternate options? My client manages the entire life cycle of the drug development process, we are looking to expand within Rheumatology. With >250 clinical trials completed within the last 5 years, my client is a world leader in developing clinical trials and bringing new therapeutics to the market. If you have a clinical background in Rheumatology and experience as an investigator or experience working with clinical trials in the pharmaceutical/Biotech/CRO industry, I welcome you to read below: *Key responsibilities* * Provide medical expertise across the entire scope of clinical development and medical affairs * Develop and deliver expert training programs * Represent Medical Affairs within Legal, Medical and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients * Collaborating with our Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Ownership and oversight of strategic clinical trial progression across a variety of tumour sub-types and therapy areas. *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Rheumatology * Investigator experience in Rheumatology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Highly competitive basic salary * Company Car * Private Healthcare * Excellent bonus scheme * Senior role within a top-5 Global Health Science Company * Clear internal promotion pathway * Flexibility in terms of office location * Opportunity to travel the world * Spearhead the development of novel therapeutics *Get in touch...* * Contact: Vincenzo B. Dessena BSc. MSc. * Clinical Development and Medical Affairs Recruitment Consultant * Email: [vdessena (at) barringtonjames.com](mailto:)
Sep 15, 2021
Full time
Do you want to drive the development and commercialization of medicines that will provide treatment to patients with little or no alternate options? My client manages the entire life cycle of the drug development process, we are looking to expand within Rheumatology. With >250 clinical trials completed within the last 5 years, my client is a world leader in developing clinical trials and bringing new therapeutics to the market. If you have a clinical background in Rheumatology and experience as an investigator or experience working with clinical trials in the pharmaceutical/Biotech/CRO industry, I welcome you to read below: *Key responsibilities* * Provide medical expertise across the entire scope of clinical development and medical affairs * Develop and deliver expert training programs * Represent Medical Affairs within Legal, Medical and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients * Collaborating with our Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Ownership and oversight of strategic clinical trial progression across a variety of tumour sub-types and therapy areas. *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Rheumatology * Investigator experience in Rheumatology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Highly competitive basic salary * Company Car * Private Healthcare * Excellent bonus scheme * Senior role within a top-5 Global Health Science Company * Clear internal promotion pathway * Flexibility in terms of office location * Opportunity to travel the world * Spearhead the development of novel therapeutics *Get in touch...* * Contact: Vincenzo B. Dessena BSc. MSc. * Clinical Development and Medical Affairs Recruitment Consultant * Email: [vdessena (at) barringtonjames.com](mailto:)
Do you want to drive the development and commercialization of medicines that will provide treatment to patients with little or no alternate options? My client manages the entire life cycle of the drug development process, we are looking to expand within Rheumatology. With >250 clinical trials completed within the last 5 years, my client is a world leader in developing clinical trials and bringing new therapeutics to the market. If you have a clinical background in Rheumatology and experience as an investigator or experience working with clinical trials in the pharmaceutical/Biotech/CRO industry, I welcome you to read below: *Key responsibilities* * Provide medical expertise across the entire scope of clinical development and medical affairs * Develop and deliver expert training programs * Represent Medical Affairs within Legal, Medical and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients * Collaborating with our Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Ownership and oversight of strategic clinical trial progression across a variety of tumour sub-types and therapy areas. *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Rheumatology * Investigator experience in Rheumatology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Highly competitive basic salary * Company Car * Private Healthcare * Excellent bonus scheme * Senior role within a top-5 Global Health Science Company * Clear internal promotion pathway * Flexibility in terms of office location * Opportunity to travel the world * Spearhead the development of novel therapeutics *Get in touch...* * Contact: Vincenzo B. Dessena BSc. MSc. * Clinical Development and Medical Affairs Recruitment Consultant * Email: [vdessena (at) barringtonjames.com](mailto:)
Sep 15, 2021
Full time
Do you want to drive the development and commercialization of medicines that will provide treatment to patients with little or no alternate options? My client manages the entire life cycle of the drug development process, we are looking to expand within Rheumatology. With >250 clinical trials completed within the last 5 years, my client is a world leader in developing clinical trials and bringing new therapeutics to the market. If you have a clinical background in Rheumatology and experience as an investigator or experience working with clinical trials in the pharmaceutical/Biotech/CRO industry, I welcome you to read below: *Key responsibilities* * Provide medical expertise across the entire scope of clinical development and medical affairs * Develop and deliver expert training programs * Represent Medical Affairs within Legal, Medical and Regulatory review committees * Apply medical and clinical expertise to inspire internal teams and external customers * Build and develop business relationships with potential clients * Collaborating with our Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan * Ownership and oversight of strategic clinical trial progression across a variety of tumour sub-types and therapy areas. *Requirements* * Medical Doctor (M.D, MBBS, MBChB or equivalent) * PhD advantageous * Clinical specialisation (residency completion, board certification or equivalent) in Rheumatology * Investigator experience in Rheumatology clinical trials is essential * Experience in phase II-III clinical trials is advantageous * Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal * Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred *Benefits* * Highly competitive basic salary * Company Car * Private Healthcare * Excellent bonus scheme * Senior role within a top-5 Global Health Science Company * Clear internal promotion pathway * Flexibility in terms of office location * Opportunity to travel the world * Spearhead the development of novel therapeutics *Get in touch...* * Contact: Vincenzo B. Dessena BSc. MSc. * Clinical Development and Medical Affairs Recruitment Consultant * Email: [vdessena (at) barringtonjames.com](mailto:)