• Associate Director , Global

    Sanofi Group (Morristown, NJ)
    **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

    Organon & Co. (Jersey City, NJ)
    **Job Description** **The Position** The Associate Director , Global Regulatory Lead (GRL), reporting to the Executive Director , Senior Director ... projects in their assigned therapeutic area portfolio. **Responsibilities** The Associate Director will be responsible to: + Develop regulatory strategy for… more
    Organon & Co. (07/26/25)
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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 (08/08/25)
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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 (08/09/25)
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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 , Global

    Gilead Sciences, Inc. (Parsippany, NJ)
    …strategy, plans and objectives for assigned products or projects. You may act as the Global Regulatory Lead for early-stage or other programs. You will lead ... Regulatory Affairs and may serve as Regional Lead or Global Regulatory Lead on cross-functional/cross-regional Regulatory Submission Teams. Provides… more
    Gilead Sciences, Inc. (08/02/25)
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  • Associate Director Regulatory

    Abbott (Santa Clara, CA)
    …Leveraged Services team supports. **The Opportunity** The ** Associate Director Regulatory Affairs** will work for our Global Regulatory Services ... and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH). This Associate Director Regulatory Affairs may analyze broad scope… more
    Abbott (08/08/25)
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  • Associate Director

    Gilead Sciences, Inc. (Foster City, CA)
    …Description** Regulatory Affairs Labeling is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner ... learn new therapeutic areas. + Demonstrates in-depth knowledge of current global and regional trends in regulatory affairs and is able to apply this to advance… more
    Gilead Sciences, Inc. (05/23/25)
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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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