• Merck & Co. (Rahway, NJ)
    …--Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... changes the way we approach serious diseases. --The Senior Director will report to an Associate Vice...Medical Research, Mentorship, Plan of Action and Milestones (POA&M), Regulatory Affairs Compliance, Regulatory Compliance… more
    HireLifeScience (10/25/25)
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  • Merck & Co. (Rahway, NJ)
    …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director more
    HireLifeScience (10/25/25)
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  • Organon & Co. (Jersey City, NJ)
    …**The Position?** Reporting to the Director in Organon Regulatory CMC,?the Associate Principal Scientist is responsible for?developing and?implementing ... questions per established business processes and systems. + Demonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the… more
    DirectEmployers Association (10/24/25)
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  • Organon & Co. (Jersey City, NJ)
    …Reporting to the Director or Executive Director in Organon Regulatory Chemistry, Manufacturing and Controls (CMC), the Associate Principal Scientist is ... questions per established business processes and systems. + Demonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the… more
    DirectEmployers Association (10/24/25)
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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 ... in the pharmaceutical industry with at least 10+ years- experience in a regulatory affairs . + Primary experience must be managing a significant number of generic… more
    Glenmark Pharmaceuticals Inc., USA (08/15/25)
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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 Regional ... role in ad hoc or special projects that continuously improve or otherwise advance Regulatory Affairs capabilities. Position will be filled in either Foster City,… more
    Gilead Sciences, Inc. (10/23/25)
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  • Associate Director , Global…

    Sanofi Group (Morristown, NJ)
    **Job Title:** Associate Director , Global Regulatory Affairs Advertising and Promotion **Location** : Cambridge, MA Morristown, NJ **About the Job** Are ... 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 (10/24/25)
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  • Global Regulatory Affairs Device…

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

    AbbVie (Florham Park, NJ)
    …and effectively, throughout the product lifecycle and the patient's journey. The Associate Scientific Director provides medical and scientific strategic and ... discovery, statistics, regulatory , etc.) as they relate to on-going medical affairs projects. + May assist as consultant and liaison with other corporations when… more
    AbbVie (10/25/25)
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  • GRA Device Lead ( Associate Director

    Sanofi Group (Morristown, NJ)
    **Job Title:** GRA Device Lead ( Associate Director ) **Location** : Morristown, NJ/ Cambridge, MA/ Framingham, MA **About the Job** Are you ready to shape the ... could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting the medical… more
    Sanofi Group (09/23/25)
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  • Associate Director , HCP and IRA…

    Teva Pharmaceuticals (Parsippany, NJ)
    Associate Director , HCP and IRA Channel Marketing Date: Oct 24, 2025 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: ... people to make a difference with. **The opportunity** The Associate Director , HCP & IRA Channel Marketing...Partner closely with Field Sales, Value and Access, Government Affairs , Finance, Forecasting / Analytics, Medical Affairs ,… more
    Teva Pharmaceuticals (10/25/25)
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  • Associate Director , Marketing…

    Sanofi Group (Morristown, NJ)
    **Job Title:** Associate Director , Marketing - Care Pathway Education T1D **Location:** Remote/Field **About the Job** The Associate Director , Marketing ... and education across endocrinology, primary care, and health system settings. The Associate Director will translate brand vision into scalable field enablement… more
    Sanofi Group (10/09/25)
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  • Associate Director , Statistics…

    AbbVie (Florham Park, NJ)
    …Specific areas of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with ... YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , Statistics - Immunology provides statistical leadership… more
    AbbVie (10/15/25)
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  • Associate Director , Global…

    Bristol Myers Squibb (Madison, NJ)
    …at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director , Global Regulatory Strategy, Neuroscience** **Position ... PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** + Understanding… more
    Bristol Myers Squibb (08/28/25)
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  • Associate Director , Iberdomide…

    Bristol Myers Squibb (Madison, NJ)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary:** The Associate Director , Iberdomide marketing will play a critical role ... initiatives, and sales force readiness activities + Coordinate closely with medical affairs and regulatory teams on scientific communications and thought leader… more
    Bristol Myers Squibb (10/23/25)
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  • Associate Director Federal Account…

    Teva Pharmaceuticals (Parsippany, NJ)
    Associate Director Federal Account Management VA DoD - Remote Date: Oct 23, 2025 Location: Parsippany, United States, New Jersey, 07054 Company: Teva ... a difference, and new people to make a difference with. **The opportunity** The Associate Director of Federal Account Management reports to the Senior … more
    Teva Pharmaceuticals (09/25/25)
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  • Associate Director , Non-Clinical…

    Organon & Co. (Jersey City, NJ)
    …development programs with early clinical development, late-clinical development, regulatory affairs , safety and pharmacovigilance, Chemistry, Manufacturing ... and Controls (CMC), medical affairs and business development. Non-Clinical Safety Assessment Representative is...for reviewing and authoring non-clinical and clinical modules for regulatory submissions, briefing books and other regulatory more
    Organon & Co. (10/25/25)
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  • Associate Director , Biostatistics…

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …representing the company in professional associations, conferences, and publications. As an Associate Director , the incumbent will be responsible for mentoring ... Clinical sub-teams. + Interact with Medical Directors, Clinical Scientists, Regulatory Affairs , Preclinical scientists, Statistical Programming, Data Management,… more
    Regeneron Pharmaceuticals (08/27/25)
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  • Associate Director , Global…

    Regeneron Pharmaceuticals (Sleepy Hollow, NY)
    The Associate Director of Global LCM Marketing will drive lifecycle management strategies to ensure long-term commercial success. This key contributor will lead ... strategy for new indications and lifecycle initiatives + Collaborate with medical affairs to develop disease area education programs for areas of high unmet… more
    Regeneron Pharmaceuticals (10/24/25)
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  • Senior Clinical Director , Oncology Early…

    Merck (Rahway, NJ)
    …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... changes the way we approach serious diseases. The Senior Director will report to an Associate Vice...Medical Research, Mentorship, Plan of Action and Milestones (POA&M), Regulatory Affairs Compliance, Regulatory Compliance… more
    Merck (10/25/25)
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