• Director Global Regulatory

    Takeda Pharmaceuticals (Boston, MA)
    …understands probabilities of technical success for the solutions. + Effectively represent the Global Regulatory Affairs (GRA) function in senior level ... for providing strategic guidance and oversight for the delivery of global regulatory strategies to support development of biomarkers, diagnostic tests, devices… more
    Takeda Pharmaceuticals (04/29/25)
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  • Senior Director , Global

    Takeda Pharmaceuticals (Lexington, MA)
    …and approves - as needed - technical protocols, reports, etc. to ensure alignment with global regulatory requirements and standards. + When in a GRA CMC Product ... tactical regulatory guidance to product teams in line with global regulatory strategies. Accountable for development and / or commercial products approvals… more
    Takeda Pharmaceuticals (04/30/25)
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  • Associate Director , Regulatory

    Rhythm Pharmaceuticals (Boston, MA)
    …commercialization and life cycle of Rhythm products. This role reports into the Director , Global Regulatory Affairs . Responsibilities and Duties ... to overcome barriers, together. Opportunity Overview In the Associate Director , Regulatory Affairs role, you...execution of regulatory filings, maintaining compliance with global regulatory standards and commitments. You will… more
    Rhythm Pharmaceuticals (03/19/25)
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  • Director , RA Global

    AbbVie (Waltham, MA)
    …Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Director Regulatory Affairs Global Regulatory ... approval for product(s) in the assigned therapeutic area. Leads the Global Regulatory Product Team (GRPT). Continually expands TA knowledge, and ensures… more
    AbbVie (04/04/25)
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  • Medical Director , Global Medical…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …and real-world evidence, US and global commercial teams, market access, and regulatory affairs , to ensure integrated global strategies and cohesive ... experienced Medical Director of CNS Early Assets, Global Medical Affairs , responsible for certain assets...or early development (phase 1) assets either within Medical Affairs , Regulatory Affairs , or Clinical… more
    Otsuka America Pharmaceutical Inc. (04/17/25)
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  • Executive Director , Regulatory

    Regeneron Pharmaceuticals (Cambridge, MA)
    …might look like: + Responsible for the strategic company guidance on FDA and global regulatory requirements ( affairs and CMC) for investigational and ... this key leadership role, you will build and oversee Global Regulatory Science and Regulatory ...position you will build and lead a cell medicine regulatory affairs team and provide regulatory more
    Regeneron Pharmaceuticals (04/11/25)
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  • Global Medical Affairs Senior…

    Sanofi Group (Cambridge, MA)
    **Job Title:** Global Medical Affairs Senior Director Kevzara **Grade:** L4-2 **Location** : Cambridge, MA **About the Job** In order to pursue Sanofi's ... engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs ...that address highest unmet needs. We are an innovative global healthcare company, committed to transforming the lives of… more
    Sanofi Group (04/03/25)
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  • Associate Director , Global Medical…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    **Position Overview** Otsuka is seeking an exceptional Associate Director of Global Medical Affairs (GMA) Excellence & Operations to support our emerging ... and tools to enhance productivity and data management within Global Medical Affairs + Develop and track...Assurance** + Ensure all GMA operations activities comply with global regulatory requirements and company policies +… more
    Otsuka America Pharmaceutical Inc. (04/17/25)
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  • Associate Director , Regulatory

    Bristol Myers Squibb (Cambridge, MA)
    …more: careers.bms.com/working-with-us . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of ... + Ensure global development plans will meet global regulatory requirements by soliciting and integrating...with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience… more
    Bristol Myers Squibb (05/03/25)
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  • Associate Director , Regulatory

    Takeda Pharmaceuticals (Boston, MA)
    … vaccine programs in various stages of development + Represents the vaccine regulatory affairs team on cross-functional Takeda Vaccines teams to ensure that ... product developmentprogramspreferred + Sound understanding of scientific principles and regulatory CMC requirements relevant to global vaccine development,… more
    Takeda Pharmaceuticals (02/22/25)
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