• Associate Director , Global Medical…

    System One (Raritan, NJ)
    Title: Associate Director , Global Medical Affairs Strategy and Execution Location: Must be local Raritan, NJ and required to go onsite 2-3 days a week Type: ... a part of this groundbreaking work, please apply! The Associate Director , Global Medical Affairs ...of proven experience is required. Experience in a medical, clinical or scientific environment is required. + Project leadership… more
    System One (08/03/25)
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  • Associate Director , Global…

    Sanofi Group (Morristown, NJ)
    **Job Title:** Associate Director , Global Regulatory Affairs - Global Labeling Strategy **Location** : Morristown, NJ or Cambridge, MA (Hybrid) **About the ... Your skills could be critical in helping our teams accelerate progress. The Associate Director , Global Regulatory Affairs - Global Labeling Strategy… 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 or ... strategies for projects in their assigned therapeutic area portfolio. **Responsibilities** The Associate Director will be responsible to: + Develop regulatory… more
    Organon & Co. (07/26/25)
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  • Associate Director , Commercial…

    Bristol Myers Squibb (Princeton, NJ)
    …Read more: careers.bms.com/working-with-us . **Description:** The role of Associate Director of US Commercial Regulatory Affairs requires the ability to ... regulatory advice, risk assessment and mitigation strategies to Commercial Teams, Medical Affairs , Public Affairs , Value Access and Payment, and other internal… more
    Bristol Myers Squibb (08/25/25)
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  • Associate Director , Medical…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …communicate with FDA and international authorities to support safety, efficiency, and clinical performance claims. + Global Medical Affairs Support: Ensure ... team in SM business unit, guiding compliance, product development, and clinical validation. **Key Responsibilities:** + Strategic Medical Leadership: Drive medical … more
    BD (Becton, Dickinson and Company) (06/29/25)
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  • Director , SM Medical Affairs , LSM…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …partner closely with the LSM worldwide business team, regional leadership in the Medical Affairs Function and the Associate Director of Medical Affairs ... directly to the business unit Vice President of Medical Affairs , the Director of Medical Affairs...align and prioritize product development, product improvement, education, and clinical study plans to support SM's value-based strategy. S/he… more
    BD (Becton, Dickinson and Company) (06/18/25)
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  • Associate Director , Regulatory…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    **Job Description Summary** As Associate Director , Regulatory Affairs , you will be responsible for leading RA team members involved in device project ... degree preferred; medical training preferred. + Minimum 8 years of regulatory affairs experience within the pharmaceutical or medical device industries, ideally with… more
    BD (Becton, Dickinson and Company) (08/27/25)
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  • Associate Director Regulatory…

    Amneal Pharmaceuticals (Piscataway, NJ)
    …Global Regulatory Strategies: Formulate and lead global CMC and clinical regulatory strategies for Biologics, Biosimilars, and Small Molecules.Ensure alignment ... with regulatory trends, innovation, and compliance while balancing business benefits and risks. + Lead and Manage Global Regulatory Submission Activities: Oversee submission planning, authoring, reviewing, and coordination for regulatory filings (eg, BLA,… more
    Amneal Pharmaceuticals (08/15/25)
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  • Associate Principal Scientist, Regulatory…

    Organon & Co. (Jersey City, NJ)
    **Job Description** **The Position** The Associate Principal Scientist ( Associate Director ) is responsible for developing and implementing Regulatory ... in accordance with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and submission of CMC… more
    Organon & Co. (07/22/25)
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  • Senior Clinical Director , Oncology…

    Merck (Rahway, NJ)
    …way we approach serious diseases. The Senior Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance ... in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and Assist the Executive Director /AVP in… more
    Merck (08/12/25)
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