• Sr. Global Director Medical Affairs (GDMA)…

    Merck (Boston, MA)
    …, Medical Research, Medical Review, Medical Writing, Patient Advocacy, Pharmaceutical Medical Affairs , Project Management, Project Management Improvement, ... **Job Description** **Role Summary:** The Sr. Global Director Medical Affairs (GDMA) is responsible for supporting the execution of scientific & medical affairs more
    Merck (08/22/25)
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  • US Executive Director, Medical Affairs

    Merck (Boston, MA)
    …Team Leadership, Executive Leadership, Healthcare Delivery Systems, Medical Affairs , Pharmaceutical Compliance, Scientific Communications, Scientific Exchange, ... **Job Description** The Executive Director (ED) for US Medical Affairs (USMA) understands Our Company's enterprise level strategies and leads cross-functionally with… more
    Merck (08/20/25)
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  • Director, US Regulatory Affairs

    Sanofi Group (Cambridge, MA)
    …and responsibilities. **About You** **Experience:** + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs + Successful track record ... **Job Title:** Director, US Regulatory Affairs - Advertising and Promotion **Location:** Cambridge, MA or Morristown, NJ **About the job** Are you ready to shape the… more
    Sanofi Group (08/08/25)
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  • Associate Director, Scientific Communications…

    Takeda Pharmaceuticals (Boston, MA)
    …of experience with the development and execution of medical publications, within medical affairs in the pharmaceutical or biotech industry or within a medical ... deliver your best. As part of the Global Medical Affairs Oncology team, you will report to the Scientific...in a scientific discipline plus commensurate long-term experience within pharmaceutical or biotech industry + 5+ years healthcare or… more
    Takeda Pharmaceuticals (07/02/25)
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  • Oncology Regional Medical Scientific Associate…

    Merck (Boston, MA)
    …, Medical Knowledge, Medical Marketing Strategy, Multiple Therapeutic Areas, Pharmaceutical Medical Affairs , Scientific Communications, Scientific Exchange, ... therapeutic area. **Research** + Upon request from Global Center for Scientific Affairs (GCSA), + Initiates discussions with SLs and/or potential investigators that… more
    Merck (08/23/25)
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  • Regional Medical Scientific Director (Medical…

    Merck (Boston, MA)
    …Research, Clinical Trials, Drug Launches, Hospital Medicine, Management Process, Medical Affairs , Pharmaceutical Medical Affairs , Scientific Research, Social ... therapeutic area. **Research** Upon request from Global Center for Scientific Affairs (GCSA), + Initiates discussions with SLs and/or potential investigators that… more
    Merck (08/13/25)
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  • Senior Principle Scientist, Regulatory Liaison…

    Merck (Boston, MA)
    …Immunology, Immunotherapy, International Regulatory Compliance, Leadership, Motivation Management, Pharmaceutical Regulatory Affairs , Regulatory Affairs ... Coordinate regional regulatory strategy and submissions through collaboration with Regulatory Affairs Europe (RAE) and local affiliate teams. + Provide final… more
    Merck (08/23/25)
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  • Compliance Operations Lead, Associate Director…

    Takeda Pharmaceuticals (Boston, MA)
    …3 years of experience in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, ... 7 years of increasing responsibility and relevant experience in the global pharmaceutical industry in functions such as Clinical Operations, Data Management and… more
    Takeda Pharmaceuticals (08/08/25)
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  • Associate Director, Clinical and Safety Quality…

    Takeda Pharmaceuticals (Boston, MA)
    …3 years of experience in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, ... 7 years of increasing responsibility and relevant experience in the global pharmaceutical industry in functions such as Clinical Operations, Data Management and… more
    Takeda Pharmaceuticals (07/25/25)
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  • Associate Director, Clinical Program Quality…

    Takeda Pharmaceuticals (Boston, MA)
    …3 years of experience in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, ... 7 years of increasing responsibility and relevant experience in the global pharmaceutical industry in functions such as Clinical Operations, Data Management and… more
    Takeda Pharmaceuticals (07/16/25)
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