• Executive Director of R&D Global Quality…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …of clinical facility and system audits at all relevant facilities, investigator sites, and vendors (including contract research organizations) and ensure that ... through the Management Review process to ensure alignment with Company policy and strategy and gain a consensus of...ensure R&D Management Reviews are conducted per QSR and Company requirements. + **Budget Management:** Develop and manage the… more
    Otsuka America Pharmaceutical Inc. (06/13/25)
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  • Global Director, Medical Affairs

    Organon & Co. (Jersey City, NJ)
    …address life cycle management needs; advise on areas of interest for investigator -initiated trials. + Lead the development and execution of medical education ... + Ensure compliance with all relevant regulations, guidelines, and company policies in the execution of medical activities. +...best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for… more
    Organon & Co. (07/24/25)
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  • Director, Medical Affairs

    Abbott (Princeton, NJ)
    …a full life. You'll also have access to:** **Career development with an international company where you can grow the career you dream of .** **Free medical coverage ... benefit - an affordable and convenient path to getting a bachelor's degree.** **A company recognized as a great place to work in dozens of countries around the… more
    Abbott (07/18/25)
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  • Clinical Research Director

    Sanofi Group (Morristown, NJ)
    …methodologies and pro-actively progress study execution. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve ... people's lives. We're also a company where you can flourish and grow your career,...regulations. + Review documents supporting clinical development such as Investigator 's brochure, regulatory documents for IND/CTA, clinical sections of… more
    Sanofi Group (07/06/25)
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  • Sr. Director/VP/Clinical Delivery Lead, Advisory…

    Norstella (Trenton, NJ)
    Sr. Director/VP/Clinical Delivery Lead, Advisory Services Company : Citeline Location: Remote, United States Date Posted: Jun 2, 2025 Employment Type: Full Time Job ... planning and forecasting + Protocol Design, Country, Site and Investigator Feasibility + Clinical trials operations, cost benchmarking &...Life and AD&D Benefits + 401k Retirement Plan with Company Match + Company Paid Short &… more
    Norstella (06/03/25)
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  • Associate Director, Global TA Regulatory Liaisons

    Gilead Sciences, Inc. (Parsippany, NJ)
    …amendment, and routine submissions (eg, Development Safety Update Reports / DSURs, Investigator Brochure/ IB updates, etc.). + Oversees and approves the authoring of ... on role), paid time off, and a benefits package. Benefits include company -sponsored medical, dental, vision, and life insurance plans*. For additional benefits… more
    Gilead Sciences, Inc. (08/02/25)
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  • Scientific/Medical Director, Medical Affairs…

    AbbVie (Florham Park, NJ)
    Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical ... analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses.… more
    AbbVie (07/26/25)
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  • Senior Clinical Research Director, I&I

    Sanofi Group (Bridgewater, NJ)
    **About the Job** We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a ... company where you can flourish and grow your career,...and/or contribute in the the clinical section of the Investigator 's brochure, CTA, IND, DSUR, INDAR, DRMP, RMP +… more
    Sanofi Group (07/06/25)
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  • Clinical Research Director, I&I

    Sanofi Group (Morristown, NJ)
    …methodologies and pro-actively progress study execution. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve ... people's lives. We're also a company where you can flourish and grow your career,...regulations + Review documents supporting clinical development such as Investigator 's brochure, regulatory documents for IND/CTA, clinical sections of… more
    Sanofi Group (07/03/25)
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  • Global Safety Officer, Rare

    Sanofi Group (Morristown, NJ)
    …in helping our teams accelerate progress. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's ... lives. We're also a company where you can flourish and grow your career,...development documents including clinical development plans, SAPs, study protocols, investigator brochures, data monitoring plans, study reports, integrated summary… more
    Sanofi Group (06/05/25)
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