• Global Project Head, Rare

    Sanofi Group (Morristown, NJ)
    …the GPH will be responsible for the communication strategy and scientific disclosures, travel authorizations, expense reports and other documents related to ... listed below, as well as all other duties assigned. ** Scientific and technical Expertise:** + Has and maintains deep...close collaboration with Market Access, Global Commercial and Medical Affairs , as Active member of GPT. + Contributor to… more
    Sanofi Group (07/30/25)
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  • Clinical Study Physician

    Teva Pharmaceuticals (Parsippany, NJ)
    …the study team and CDT. The CTP is expected to advance scientific and clinical knowledge, incorporate new methodologies, and pro-actively progress study execution. ... assignment) with demonstrated decision-making capabilities + Provides medical and scientific expertise to cross-functional colleagues Travel Requirements: Approximately 20%,… more
    Teva Pharmaceuticals (10/07/25)
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  • Senior Manager, Worldwide Medical Hematology,…

    Bristol Myers Squibb (Princeton, NJ)
    …reports to the Director of Medical Communications within WWMH, of Global Medical Affairs and is responsible for the planning and timely execution of scientifically ... develop and timely delivery of strategically aligned medical publications, scientific content, medical information, medical education, training content, and congress… more
    Bristol Myers Squibb (09/11/25)
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  • US Transplant Medical Program Lead (MPL)

    Sanofi Group (Morristown, NJ)
    …needs. The MPL will also be responsible to lead the local scientific review process (eg, local concept/protocol review) and all subsequent applicable aspects ... management with internal and external stakeholders: US and Global Medical Affairs , NA Corporate Integrity Agreement Monitors, Legal, Regulatory, Finance, Ethics &… more
    Sanofi Group (09/30/25)
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  • Field Director, Medical Science Liaison…

    Grifols Shared Services North America, Inc (Atlantic City, NJ)
    …ensures compliant execution of field medical plans, strategy, and activities within Medical Affairs , as aligned with goals and objectives. This position is a remote ... but are not limited to:_ + Ultimate responsibility for scientific knowledge of self/team and oversight of a team...Directors, National MSL Sr Director, and North America Medical Affairs Sr Director to develop field medical strategies and… more
    Grifols Shared Services North America, Inc (07/24/25)
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  • GRA Device Lead (Director)

    Sanofi Group (Morristown, NJ)
    …portfolio of products. The team is part of the Global Regulatory Affairs , Regulatory CMC and Device Department within Global Research and Development. Sanofi's ... global regulatory affairs (GRA) function is comprised of more than 1800...professional global environment. **Skills/Qualifications:** + MS degree -in a scientific or engineering discipline -with 6 years regulatory experience,… more
    Sanofi Group (07/15/25)
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  • Senior Director, Multiple Myeloma, GPRC5D

    Bristol Myers Squibb (Princeton, NJ)
    …Pipeline Lead, the Senior Director, Multiple Myeloma, GPRC5D will represent WW Medical Affairs as therapeutic area expert and provide scientific leadership and ... ensure launch readiness globally + Collaborate with local medical affairs teams to align on launch strategy and tactics,...congresses such as COMy, EHA, and IMS, to enhance scientific dialogue + Refine Integrated Evidence Plan (IEP) to… more
    Bristol Myers Squibb (10/06/25)
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  • GRA Device Lead (Associate Director)

    Sanofi Group (Morristown, NJ)
    …could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting the medical device, ... creates and maintains strong collaborative working relationships with Global Regulatory Affairs (GRA), Regional GRA, Country Regulatory Groups, Technical and Quality… more
    Sanofi Group (09/23/25)
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  • GRA Device Lead (Associate Director)

    Sanofi Group (Morristown, NJ)
    …could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting the medical device, ... creates and maintains strong collaborative working relationships with Global Regulatory Affairs (GRA), Regional GRA, Country Regulatory Groups, Technical and Quality… more
    Sanofi Group (09/20/25)
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  • Director, MEG Lead Hematology, Medical Evidence…

    Bristol Myers Squibb (Madison, NJ)
    …Hematology portfolio, including Clinical Research Collaborations (CRCs), Medical Affairs Sponsored Studies (MAST), and Investigator-Sponsored Research Studies ... between BMS and thought leaders in community practice and academia, including scientific dialogue and representing BMS as a trusted, inclusive, and innovative… more
    Bristol Myers Squibb (09/11/25)
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