• Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    …Payer Marketing and Market Access, Global Evidence and Outcomes, Medica Affairs , Clinical Development, Regulatory Affairs , Biostatistics, Global ... Market Access, Pricing, Advocacy, Biostatistics, Global Evidence and Outcomes, Medical Affairs , Clinical Science, Legal, Regulatory + OBU 10, EUCAN, GEM… more
    Takeda Pharmaceuticals (09/30/25)
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  • Associate Director

    Gilead Sciences, Inc. (Parsippany, NJ)
    …Join Gilead and help create possible, together. **Job Description** As an Associate Director , Global Regulatory Affairs , you will act as the ... Affairs and may serve as Regional Regulatory Lead or Global Regulatory ...current global and regional trends in biopharmaceutical regulatory affairs . Proven effectiveness applying this knowledge… more
    Gilead Sciences, Inc. (10/23/25)
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  • Associate Director , Program…

    AbbVie (Barceloneta, PR)
    …Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The ME&C Associate Director is a global program management expert ... to use their broad understanding of Product Development, Manufacturing, Quality and Regulatory Affairs to translate the business objectives into actionable… more
    AbbVie (11/15/25)
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  • Associate Director

    Sumitomo Pharma (Lincoln, NE)
    Affairs (Oncology).** The Associate Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/She will primarily function ... as a regional regulatory leader (RRL) and/or Global ...Ideally with a minimum of 4 years focused in regulatory affairs + Oncology product development experience… more
    Sumitomo Pharma (10/11/25)
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  • Manager | Associate Director

    Boehringer Ingelheim (St. Joseph, MO)
    …meetings, planning activities and FDA communications. Associate Director Act as Regulatory Affairs ( RA ) core or subteam member in projects as well ... **Description** Manager The Manager, Regulatory Affairs ( RA ) Pharma...as defined. + Supports specific infrastructural projects as assigned. Associate Director + Responsibility for the safety… more
    Boehringer Ingelheim (10/29/25)
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  • Global Regulatory Affairs

    Sanofi Group (Morristown, NJ)
    **Job title** : Global Regulatory Affairs Device Lead ( Associate Director ) **Location** : Morristown, NJ or Cambridge, MA or Framingham, MA **About ... Your skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting… more
    Sanofi Group (10/23/25)
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  • Associate Director

    AbbVie (North Chicago, IL)
    …Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director Regulatory Affairs , Chemistry, ... affairs on teams such as the product development, Global Regulatory Product Teams and Operations brand...documents policies and procedures within the regulatory affairs department. Leads initiatives internal to RA more
    AbbVie (10/29/25)
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  • Associate Director

    Glenmark Pharmaceuticals Inc., USA (Elmwood Park, NJ)
    Associate Director , Regulatory Affairs Department: Regulatory Affairs Location: Elmwood Park, NJ START YOUR APPLICATION ... post-approval work. Form 2252 for Annual Reports. + Provide support/ RA strategy needed to achieve timely approvals with the...industry with at least 10+ years- experience in a regulatory affairs . + Primary experience must be… more
    Glenmark Pharmaceuticals Inc., USA (11/14/25)
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  • Associate Director

    Rhythm Pharmaceuticals (Boston, MA)
    …commercialization and life cycle of Rhythm products. This role reports into the Director , Global Regulatory Affairs . Responsibilities and Duties ... tenacity to overcome barriers, together. Opportunity Overview In the Associate Director , Regulatory Affairs...execution of regulatory filings, maintaining compliance with global regulatory standards and commitments. You will… more
    Rhythm Pharmaceuticals (09/17/25)
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  • Associate Director

    Merck (Rahway, NJ)
    Regulatory Innovation and Information Management (RIIM) within Global Regulatory Affairs & Clinical Safety (GRACS) The Associate Director of ... **Job Description** ** Associate Director , Regulatory Submissions...requirements, workflows, and metadata standards. + Ensure compliance with global regulatory standards and internal SOPs for… more
    Merck (11/22/25)
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