• Associate Director , Regulatory

    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 for ... and life cycle of Rhythm products. This role reports into the Director , Global Regulatory Affairs . Responsibilities and Duties + Act as the Global… more
    Rhythm Pharmaceuticals (06/18/25)
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  • Director , Regulatory Affairs

    BeOne Medicines (Cambridge, MA)
    BeOne Medicines USA, Inc. (f/ka BeiGene) seeks Director , Regulatory Affairs in Cambridge, MA, USA: **Job Duties:** + Provides high level regulatory ... direction and mentorship on projects including, but not limited to general regulatory strategies, regulatory requirements for clinical studies and marketing… more
    BeOne Medicines (07/03/25)
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  • Associate Director , Global…

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

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

    Takeda Pharmaceuticals (Boston, MA)
    …is possible in order to bring life-changing therapies to patients worldwide. The Director Global Regulatory Affairs , Neuroscience is responsible for ... appropriate regulatory strategy. + Participates in cross-functionalinitiativeswithin Global Regulatory Affairs and Takeda R&D. **How you will contribute:**… more
    Takeda Pharmaceuticals (07/02/25)
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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 ... medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion lead you will act… more
    Takeda Pharmaceuticals (08/03/25)
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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, ... therapies to patients worldwide. Join Takeda as an Associate Director , GRA CMC Small Molecules where you will oversee...where you will oversee the development and execution of regulatory CMC development and registration strategies. You will be… more
    Takeda Pharmaceuticals (07/08/25)
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  • Associate Director , Global…

    Sanofi Group (Cambridge, MA)
    **Job Title:** Associate Director , Global Regulatory Affairs Advertising and Promotion **Location** : Cambridge, MA Morristown, NJ **About the Job** Are you ... was possible. Ready to get started?​ **Main Responsibilities:** + Represents Global Regulatory Affairs (US RA AdPromo) as a member of cross-functional brand and… more
    Sanofi Group (07/30/25)
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  • Executive Director , Regulatory

    Regeneron Pharmaceuticals (Cambridge, MA)
    …stem cell transplant. In this position you will build and lead a cell medicine regulatory affairs team and provide regulatory leadership and oversight to the ... development of innovative regulatory affairs and CMC regulatory ...and internal stakeholders. A typical day as an Executive Director might look like: + Responsible for the strategic… more
    Regeneron Pharmaceuticals (07/11/25)
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  • Associate Director , Regulatory

    United Therapeutics (Boston, MA)
    …or pharma regulatory experience with a Bachelor's Degree in life sciences, quality, regulatory affairs or a related area of study or 10+ years of biologic ... pharma regulatory experience with a Master's Degree in life sciences, quality, regulatory affairs or a related area of study or 7+ years of biologic or… more
    United Therapeutics (06/14/25)
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