• Associate Director , Global

    Organon & Co. (Jersey City, NJ)
    **Job Description** **The Position** The Associate Director , Global Regulatory Lead (GRL), reporting to the Executive Director , Senior Director or ... or the EU-procedure regulatory expert on those projects. + Lead the Global Regulatory Teams, which coordinates cross-functional regulatory support for… more
    Organon & Co. (07/26/25)
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  • Associate Director , Global

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

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

    Takeda Pharmaceuticals (Boston, MA)
    …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...Takeda R&D. **How you will contribute:** + The Associate Director will be responsible for increasingly complex or multiple… more
    Takeda Pharmaceuticals (08/08/25)
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  • Director , Global Regulatory

    BeOne Medicines (San Mateo, CA)
    **General Description** **_:_** + The Director , Global Regulatory Lead, will be responsible for developing, implementing, and advising on global ... development, regulatory , and registration strategies. + The Director , Global Regulatory Lead supporting programs within BeOne's Hematology Franchise,… more
    BeOne Medicines (07/17/25)
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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, ... meetings, international experience preferred. + Understanding of scientific principles and regulatory CMC requirements relevant to global drug development and… more
    Takeda Pharmaceuticals (07/08/25)
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  • Director , Global Regulatory

    Takeda Pharmaceuticals (Boston, MA)
    …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Director , Global Regulatory Labeling Strategy where you will be ... escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned products… more
    Takeda Pharmaceuticals (08/11/25)
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  • Sr. Director - Global

    Lilly (Indianapolis, IN)
    …to make life better for people around the world. **Purpose:** The purpose of the Senior Director Global Regulatory Affairs, Global Regulatory Lead ... (GRL) role is to develop and implement innovative global regulatory strategies for product(s) in the assigned therapeutic area. The GRL is the accountable… more
    Lilly (06/04/25)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    …possible in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and Promotion (GRA ... prescription medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion lead you will… more
    Takeda Pharmaceuticals (08/11/25)
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  • Senior Director , Global

    Lilly (Indianapolis, IN)
    …are determined to make life better for people around the world. **Purpose:** The Senior Director of Global Regulatory Affairs - CMC (GRA-CMC) leads and ... to lead preparation, review, and finalization of CMC documents for global regulatory submissions, including Clinical Trial Applications, Market Authorization… more
    Lilly (06/25/25)
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