• Merck & Co. (Rahway, NJ)
    …responsibilities.Proven track record in setting and delivering product strategy in regulatory affairs and pharmacovigilance domains, with an ability to ... or equivalent regulatory authoring/publishing platforms.Demonstrated experience delivering regulatory affairs and pharmacovigilance technology solutions (authoring/publishing,… more
    HireLifeScience (11/05/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …documents (eg SOPs) as appropriate.Collaborate with cross-functional teams (eg, Medical Safety , Regulatory Affairs , Epidemiology) to ensure benefit-risk ... optimize, and innovate signal detection and management processes across the global safety organization. The incumbent will ensure regulatory compliance, promote… more
    HireLifeScience (09/03/25)
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  • Organon & Co. (Jersey City, NJ)
    …cross-functional 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 responsible for strategic… more
    DirectEmployers Association (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 May Be… more
    HireLifeScience (11/12/25)
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  • Organon & Co. (Jersey City, NJ)
    **Job Description** **The Position** The role of Associate Director, Dermatology Outcomes Research Epidemiology and Economics will report to the headquarters ... Director of Medical Affairs Outcomes Research. Focusing on Dermatology, in this role, you will be responsible for establishing/continuing economic Modelling research… more
    DirectEmployers Association (10/07/25)
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  • Regulatory and Safety Affairs

    Reckitt (Parsippany, NJ)
    Regulatory and Safety Affairs Associate (Essential Home) City: Parsippany **We are Reckitt** Home to the world's best loved and trusted hygiene, health, ... to grow in our great organisation. **About the role** The Regulatory Affairs & Safety Associate , Regulatory and Compliance provides regulatory more
    Reckitt (11/04/25)
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  • Associate Director, Regulatory

    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 ... 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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  • Executive Director, Digital Regulatory

    Merck (Rahway, NJ)
    …+ Proven track record in setting and delivering product strategy in regulatory affairs and pharmacovigilance domains, with an ability to execute ... regulatory authoring/publishing platforms. + Demonstrated experience delivering regulatory affairs and pharmacovigilance technology solutions (authoring/publishing,… more
    Merck (11/05/25)
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  • Assoc Prin Scientist, Regulatory Liaison

    Merck (Rahway, NJ)
    **Job Description** Associate Principal Scientist Regulatory Affairs - Oncology At our company, we aspire to be the premier research-intensive ... Pharmaceutical Management, Process Improvement Projects, Process Improvements, Quality Management, Regulatory Affairs Management, Regulatory Communications, … more
    Merck (11/11/25)
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  • Associate Director, Global Labeling Product…

    J&J Family of Companies (Raritan, NJ)
    …and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Regulatory Affairs Group **Job Sub** **Function:** Regulatory ... is preferred. + Relevant experience in the pharmaceutical industry (eg, Regulatory Affairs , Clinical, Medical Information, Pharmacovigilance, etc.) is required.… more
    J&J Family of Companies (11/07/25)
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  • Quality Assurance Senior Associate

    System One (Bridgewater, NJ)
    Title: Regulatory /QA Sr. Associate Type: Direct Hire Location: Morris County, NJ Hours: 9am-5pm (Hybrid schedule) . Must have: + Strong experience with product ... key role in maintaining and enhancing product quality and regulatory compliance. Reporting to the Associate Director...with internal quality standards + Balance customer satisfaction with regulatory and safety compliance + Manage risk… more
    System One (10/10/25)
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  • Associate Director, ICSR Management Team…

    Ascendis Pharma (Princeton, NJ)
    Safety Databases (Argus preferred) + Experience with MedDRA coding and global safety reporting regulatory requirements. + Expert knowledge of FDA safety ... for employees to grow and develop their skills. The Associate Director, ICSR Management Team reports to the Director,... regulatory guidance documents; working knowledge of global safety regulations. + Ability to travel up to 20%… more
    Ascendis Pharma (10/09/25)
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  • Associate Director, Statistics - Immunology

    AbbVie (Florham Park, NJ)
    …of work may include clinical trials, patient safety , and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple ... and drive alignment with functional management. Partner with other functions (Clinical, Regulatory , Patient Safety , and GMA, etc.) to create development… more
    AbbVie (10/15/25)
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  • Associate Director, US Medical…

    Bristol Myers Squibb (Princeton, NJ)
    …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director, US Medical Neuropsychiatry position works in the US Medical ... points across US functional and commercialization areas to ensure alignment. The Associate Director will report to the Senior Director, US Medical Neuropsychiatry.… more
    Bristol Myers Squibb (10/30/25)
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  • Senior Director, Clinical Research,…

    Merck (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 May… more
    Merck (11/12/25)
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