• Associate Director , Global

    Sanofi Group (Cambridge, MA)
    **Job Title:** Associate Director , Global Regulatory Affairs - Global Labeling Strategy **Location** : Morristown, NJ or Cambridge, MA (Hybrid) ... families. Your skills could be critical in helping our teams accelerate progress. The Associate Director , Global Regulatory Affairs - Global Labeling… more
    Sanofi Group (06/27/25)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    …what is possible in order to bring life-changing therapies to patients worldwide. The Associate Director Global Regulatory Affairs, Neuroscience is ... responsible for developing innovative global regulatory strategies and providing strategic regulatory guidance...and Takeda R&D. **How you will contribute:** + The Associate Director will be responsible for increasingly… more
    Takeda Pharmaceuticals (05/07/25)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    …what is possible in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and ... to prescription medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion lead… more
    Takeda Pharmaceuticals (07/20/25)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    …my knowledge. **Job Description** **Objective / Purpose:** + Defines, develops and leads global strategies to maximize global regulatory success towards ... + Provides leadership and development for direct reports, including those that serve as global regulatory leads responsible for the design and execution of … more
    Takeda Pharmaceuticals (05/13/25)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    Global Regulatory Affairs CMC team, you will report to the Senior Director Global Regulatory Affairs CMC. **How you will contribute:** + Plan, ... in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , GRA CMC Small Molecules where you will oversee the… more
    Takeda Pharmaceuticals (07/08/25)
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  • Associate Director

    Rhythm Pharmaceuticals (Boston, MA)
    …learn, and our tenacity to overcome barriers, together. Opportunity Overview In the Associate Director , Regulatory Affairs role, you will be responsible ... commercialization and life cycle of Rhythm products. This role reports into the Director , Global Regulatory Affairs. Responsibilities and Duties + Act as the… more
    Rhythm Pharmaceuticals (06/18/25)
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  • Associate Director CMC…

    Regeneron Pharmaceuticals (Cambridge, MA)
    Regeneron Cell Medicine is looking for an Associate Director in Regulatory CMC for biologics who will be responsible for the development and submission of ... to regulatory health authorities. + Leads the development of global CMC regulatory science-based strategies for internal RCM oncology investigational… more
    Regeneron Pharmaceuticals (06/09/25)
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  • Associate Director , Scientific…

    Takeda Pharmaceuticals (Boston, MA)
    …the development of scientific communications strategy and deliverables, the ** Associate Director , Scientific Communications Lead, Hematology** proactively ... empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to...in life sciences, and excellent project management skills. The Associate Director , Scientific Communications Lead, develops and… more
    Takeda Pharmaceuticals (07/02/25)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    …leadership at LOC level Decision-making and Autonomy + Responsibility in line with Associate Director level position; independently lead HE projects and support ... Access, Global Evidence and Outcomes, Medica Affairs, Clinical Development, Regulatory Affairs, Biostatistics, Global Emerging Markets (GEM; eg, China),… more
    Takeda Pharmaceuticals (07/01/25)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    …is true to the best of my knowledge. **Job Description** **OBJECTIVES:** Global Evidence and Outcomes (GEO) contributes to the successful development and ... analysis plans, scientific reports, briefing packages, clinical study reports, and regulatory labelling interactions. + Provide technical expertise and guidance on… more
    Takeda Pharmaceuticals (07/16/25)
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