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Reporting directly to the Sr. Director, Global Medical & Scientific Affairs (GMSA), Abbott Point of Care. Contribution to global Medical & Scientific Affairs strategy in conjunction with Directors of EMEA and APAC Medical Affairs.
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The Senior Scientist supports the Center for Outcomes Research, Real-world Evidence and Epidemiology (CORE) team in Global Medical Affairs. Support execution of communication/publication strategies for given product & for publication/presentation of research outcomes at scientific conferences and forums.
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Nonclinical Safety (NCS), within Nonclinical Research and Biotherapeutics, is responsible for designing and implementing overall nonclinical safety strategy to support the development and eventual marketing approval and post-marketing safety for the breadth of the BMS portfolio in oncology, hematology, cardiovascular disease, fibrosis, immunology and neurology.
$231,300 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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In certain situations, may serve as chair of Core Medical Team, at the discretion of the Executive Director Represent NNI Medical Affairs on Global Core Medical Team (CMT) Collaborate with HEOR to provide clinical input on HEOR projects and authorship on abstracts, posters, and manuscripts, when requested Serve on Local Labeling Committee (LLC) and provide medical input to Regulatory Affairs.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Supporting the Director of Global Scientific Affairs, in conjunction with the Sr. Manager and Project Manager in Global Scientific Affairs, with KOL management as it relates to investigator-sponsored studies (ISS) and/or collaborative research studies (CRS.
$286,700 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Director will develop collaborative partnerships with the cross-functional Insmed team (Medical Affairs, HEOR, Clinical Development, Advocacy, Commercial and Market Access) as well as external medical experts and will have an integral role in driving the planning and execution of scientific communications deliverables across the Insmed respiratory franchise.
$250,800 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Strong scientific and academic background within clinical research, pharmaceutical experience or experimental medicine experience in the respective therapeutic area preferred. More than 5 years of clinical or scientific research experience and/or more than >10 years industry experience.
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7+ years of medical affairs or clinical development background in oncology. Collaborate with medical and clinical operations departments to coordinate the planning, execution, and management of clinical trial activities across medical affairs functions.
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Bristol-Myers Squibb is actively conducting translational medicine research to further our understanding of cancer biology and to identify which patient populations may be more likely to derive benefit from Immuno-Oncology (I-O.
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Ensure deliverables are in alignment with business strategy, medical affairs strategy and Insmed clinical development programs. Ability to interpret and organize highly complex scientific data including reviewing pre-clinical and clinical trial data and output from statistical analyses.
$250,800 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Work closely with individual clinical teams as well as functional area partners (e.g., Translational research, Precision Medicine and diagnostics, Regulatory Affairs, Market Access, Clinical Development) to identify and implement end-to-end Data Science solutions aimed at facilitating decision making.
$244,000 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Minimum requirement: 2+ years in the pharmaceutical industry, life sciences consulting or a managed care setting in the direct conduct of health economics, outcomes research, real-world evidence, and epidemiology studies.
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The role will also include working closely with our Medical and Clinical Affairs (MACA) team to recommend clinical and health economic studies and health economic data analysis as well as our Research and Development teams as we develop new products within the AWC portfolio.
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Oversee production and testing of lentivirus, retrovirus, and/or AAV at the research, process development or GMP production scale for use in clinical cell and gene therapy project activities.
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Through scientific exchange, the MSL will communicate and advance the scientific platform aligned with the overall medical communications and medical affairs strategies. Attend medical/scientific meetings to represent Zealand Medical Affairs with KOLs and other HCPs, strengthen individual expertise as well as capture, integrate, and summarize information of strategic interest.
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clinical research scientific affairs jobs Title: director Company: Regeneron Pharmaceuticals Inc in Belle Mead, NJ
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