• Associate Director…

    Sumitomo Pharma (Trenton, NJ)
    …currently seeking a dynamic, highly motivated, and experienced individual for the position of Associate Director Regulatory Affairs. The Associate ... Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/she...of the Global Regulatory Team (GRT), leads regulatory activities for assigned project (s) in line… more
    Sumitomo Pharma (11/20/25)
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  • Associate Director , Global…

    J&J Family of Companies (Raritan, NJ)
    …Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Director , Global Regulatory Affairs Diagnostics. This ... We invite candidates from any location to apply. The Associate Director , Global Regulatory Affairs...project teams regarding in vitro diagnostic regulations and regulatory strategy. + Draft and/or review the US and… more
    J&J Family of Companies (10/28/25)
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  • Associate Director…

    Sumitomo Pharma (Trenton, NJ)
    …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs (Oncology).** The Associate ... Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/She...requests. In addition, this position may represent GRA in project related meetings, develop regulatory strategy and… more
    Sumitomo Pharma (10/11/25)
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  • Associate Director…

    Merck (Rahway, NJ)
    **Job Description** ** Associate Director , Regulatory Submissions Archive Operations** Location: Rahway, NJ (Hybrid role - onsite 3 days per week required) ... (RIIM) within Global Regulatory Affairs & Clinical Safety (GRACS) The Associate Director of Regulatory Submissions Archive Operations serves as… more
    Merck (11/22/25)
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  • Global Regulatory Affairs Device Lead…

    Sanofi Group (Morristown, NJ)
    **Job title** : Global Regulatory Affairs Device Lead ( Associate Director ) **Location** : Morristown, NJ or Cambridge, MA or Framingham, MA **About the Job** ... critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse...Responsibilities** + Serve as GRA Device Lead on assigned project teams (early phase, late stage and marketed products)… more
    Sanofi Group (10/23/25)
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  • Associate Director…

    Gilead Sciences, Inc. (Parsippany, NJ)
    …their aspirations. Join Gilead and help create possible, together. **Job Description** As an Associate Director , Global Regulatory Affairs, you will act as ... programs. You will lead Regulatory Submission Teams or other Regulatory Project Teams and represent Global Therapeutic Area Regulatory on… more
    Gilead Sciences, Inc. (10/23/25)
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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 ... + Update the internal tracker that records all incoming and outgoing regulatory activities/communications for ANDAs/OTCs which may include submissions to FDA and… more
    Glenmark Pharmaceuticals Inc., USA (11/14/25)
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  • Associate Director , Project…

    Merck (Rahway, NJ)
    …Management Office (PMO); and Administrative Professionals. **Position Description/Summary:** The GPAM Associate Director , Value & Implementation Project ... and realize its full potential. The Associate Director is expected to provide project management... Management, Project Management Information Systems (PMIS), Project Planning, Publications Management, Regulatory Compliance, Risk… more
    Merck (11/22/25)
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  • Regulatory Affairs Associate…

    GRAIL (NJ)
    …For more information, please visit grail.com . The role assists with regulatory strategy and the development of submissions in partnership with key internal ... including Multi-Cancer Early Detection (MCED). The position supports the US Regulatory team in preparing Investigational Device Exemptions (IDEs), IDE supplements,… more
    GRAIL (11/21/25)
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  • Associate Clinical Project…

    IQVIA (Parsippany, NJ)
    **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director /Trial Delivery Manager (TDM) to lead and coordinate ... and retention of trial documents. + Provide central documents for regulatory submissions. + Support Health Authority inspections and internal audits. **Training… more
    IQVIA (10/22/25)
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