• Senior Manager, US Medical Information and Review

    Takeda Pharmaceuticals (Lexington, MA)
    …/ clinical expertise for assigned products to internal (Medical Affairs strategy teams, Therapeutic Area Units within R&D, commercial Brand teams) and ... 2-3 years of healthcare or related experience (managed markets, clinical practice, research or academic) following award...scientific languages to communicate with key Thought Leaders, Medical Affairs , Research and Development, as well as… more
    Takeda Pharmaceuticals (08/15/25)
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  • Senior Principal Scientist, Translational…

    Merck (Boston, MA)
    …(including discovery research , biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations) + ... Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout sites in the USA, UK… more
    Merck (09/03/25)
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  • Translational Sciences Lead - Immunology

    Takeda Pharmaceuticals (Boston, MA)
    …market authorization by being accountable for innovation and early discovery, non- clinical development, translational & biomarker research and bioanalytical ... also works closely with various key stakeholder functions (eg. Clinical , Clinical Operations, Medical Affairs ,...NTS team, responsible for conceptualizing, designing, and managing outsourced research and non- clinical studies at CROs to… more
    Takeda Pharmaceuticals (07/12/25)
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  • GRA Device Lead (Director)

    Sanofi Group (Cambridge, MA)
    …products. The team is part of the Global Regulatory Affairs , Regulatory CMC and Device Department within Global Research and Development. Sanofi's global ... Lead for Specialty Care Combination Products will oversee key regulatory activities and report to the GRA Device Team...The incumbent will work closely with key stakeholders including clinical , medical affairs , Industrial Affairs more
    Sanofi Group (07/15/25)
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  • Development Scientific Director, Neurology (Early…

    Sanofi Group (Cambridge, MA)
    Research Director, Safety Officer and Pharmacovigilance, Translational Medicine, Regulatory Affairs , Biostatistics, Clinical Study Units, Medical ... + Strong scientific and clinical development expertise, especially in neurology. Clinical research and drug development expertise in Alzheimer's disease is… more
    Sanofi Group (08/21/25)
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  • Medical Science Liaison

    US Tech Solutions (Cambridge, MA)
    …scientific content and context to multiple audiences.** + Fundamental understanding of clinical research + **Excellent project management** ability + Excellent ... + Build and cultivate working relationships across internal stakeholders (Medical Affairs colleagues, Clinical Operations, HEOR, R&D, Medical Information and… more
    US Tech Solutions (09/08/25)
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  • Director, US Medical, New Product Planning

    Takeda Pharmaceuticals (Lexington, MA)
    …working on cross-functional teams and project management + Experience with clinical research , publication activities, congress presentations, and public speaking ... degreed professionals considered depending on past relevant pharmaceutical industry experience, and/or clinical work, research , or academic endeavors Experience… more
    Takeda Pharmaceuticals (08/28/25)
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  • Head of Global Scientific Communications…

    Takeda Pharmaceuticals (Cambridge, MA)
    …of regulatory guidelines and compliance requirements relevant to medical affairs activities. + Proven leadership and people management skills and the ability ... areas strategy. This individual will engage with cross-functional partners including research , medical, commercial brand teams, alliance and strategic partners, and… more
    Takeda Pharmaceuticals (07/15/25)
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  • Associate Director, Global Health Economics Lead,…

    Takeda Pharmaceuticals (Boston, MA)
    …and Market Access, Global Evidence and Outcomes, Medica Affairs , Clinical Development, Regulatory Affairs , Biostatistics, Global Emerging Markets ... Interaction + Market Access, Pricing, Advocacy, Biostatistics, Global Evidence and Outcomes, Medical Affairs , Clinical Science, Legal, Regulatory + OBU 10,… more
    Takeda Pharmaceuticals (07/01/25)
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  • Global Project Head, Rare

    Sanofi Group (Cambridge, MA)
    …dotted-line management toward all GPT members, including eg project management, clinical operations, regulatory , safety, translational medicine, statistics, CMC, ... The GPH will be delegated such responsibilities as interaction with regulatory /health authorities (HA), approval of documents and product label, as appropriate.… more
    Sanofi Group (07/30/25)
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