• Merck & Co. (Rahway, NJ)
    …DescriptionThe GRACS Global Process Lead (GPL) is responsible for overseeing and managing Global Regulatory Affairs & Clinical Safety (GRACS) global ... effective, and compliant business standards, process maps, and risk management for global processes across GRACS. The GPL actively engages with leadership across the… more
    HireLifeScience (09/07/24)
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  • Eisai, Inc (Nutley, NJ)
    …health economics and outcomes research strategies, timelines and budgets with medical affairs , marketing, market access and global value and access teams. ... If this is your profile, we want to hear from you.Job Summary The Director is responsible for developing strategies for assigned product(s) and execution of HEOR and… more
    HireLifeScience (08/22/24)
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  • Merck & Co. (Rahway, NJ)
    …pharmaceutical, life sciences and/or healthcare space Understanding and experience with global regulatory requirements for Medical Device and/or AI algorithms ... diagnostics and pharma? Then you could be our new Global Marketing Director of Digital Diagnostics! -...stakeholders across HH, our Research & Development Division, Medical Affairs , Regulatory , Legal etc. as well as… more
    HireLifeScience (08/28/24)
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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 ... regulatory filing, and publication. Specifically, The Senior Clinical Director May Be Responsible For: Evaluating pre-clinical and translational work for… more
    HireLifeScience (08/27/24)
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  • Merck & Co. (Rahway, NJ)
    … may:Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Job DescriptionThe Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving… more
    HireLifeScience (08/27/24)
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  • Merck & Co. (Rahway, NJ)
    …studies;Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... Job DescriptionOur company is a global health care leader with a diversified portfolio...of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director more
    HireLifeScience (08/31/24)
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  • Merck & Co. (Rahway, NJ)
    …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May… more
    HireLifeScience (08/27/24)
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  • Director Global Regulatory

    Merck (Rahway, NJ)
    **Job Description** Our Diagnostics focused Regulatory Affairs team helps bring new precision medicine advancements to the world by facilitating effective, ... as appropriate, and corresponding therapeutic dossiers. + Interacting with global regulatory authorities and diagnostic partners to...devices, the majority of which must be in diagnostic regulatory affairs . Preferred: MS with minimum of… more
    Merck (08/14/24)
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  • Director , Global Regulatory

    Merck (Rahway, NJ)
    …The GRACS Global Process Lead (GPL) is responsible for overseeing and managing Global Regulatory Affairs & Clinical Safety (GRACS) global business ... compliant business standards, process maps, and risk management for global processes across GRACS. The GPL actively engages with...+ Complete Impact assessment on new or changed external regulatory policies as it pertains to the processes that… more
    Merck (09/07/24)
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  • Regulatory Affairs Sr Manager…

    Vantage Specialty Chemicals (Fairfield, NJ)
    … compliance in Personal Care and Cosmetics. This position will report directly to the Global Director Regulatory Affairs . The person will be responsible ... it here. For more information visit: www.vantagegrp.com or LinkedIn/vantage **POSITION SUMMARY** Regulatory Affairs Senior Manager is responsible for leading the… more
    Vantage Specialty Chemicals (06/30/24)
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  • Director , Regulatory Affairs

    AbbVie (Florham Park, NJ)
    …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Director Regulatory Affairs , Strategic Labeling is responsible for ... and product labeling (CCDS, US/EU labeling documents) at Senior level meetings ( Global Regulatory Forum (GRF), Executive Labeling Committee (ELC), Steering… more
    AbbVie (09/10/24)
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  • Senior Director , Regulatory

    Mitsubishi Chemical Group (Jersey City, NJ)
    …researching on real-world evidence, and creating hope for all facing illness. The Senior Director , Regulatory Affairs - Clinical (Neuroderm), may be called ... to facilitate timely drug development and registration. The Senior Director , Regulatory Affairs - Clinical...Global Regulatory Project Teams; and represents Regulatory Affairs on various other process and… more
    Mitsubishi Chemical Group (06/26/24)
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  • Director , Regulatory Affairs

    Mitsubishi Chemical Group (Jersey City, NJ)
    …creating hope for all facing illness. The Director , Regulatory Affairs (Early Development) provides strategic global regulatory guidance to ... and guidelines. + Leads as a key member of Global Regulatory Project Teams. + Leads multidisciplinary...requests, and briefing documents. + Acts as liaison between Regulatory Affairs and other functional areas, including… more
    Mitsubishi Chemical Group (06/21/24)
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  • Director , Legal and Regulatory

    New York State Energy Research and Development Aut (New York, NY)
    …passion to work in a fast-paced environment on the cutting edge of energy policy. The Director , Legal and Regulatory Affairs will report directly to the NY ... York is leading the nation in the fight on global climate change and the transition to a clean...Bank's Managing Director , Head of Legal and Regulatory Affairs and be charged with anticipating… more
    New York State Energy Research and Development Aut (09/03/24)
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  • Director , Compliance & Ethics,…

    Teva Pharmaceuticals (Parsippany, NJ)
    Director , Compliance & Ethics, Global R&D and Medical Affairs Date: Sep 6, 2024 Location: Parsippany, United States, New Jersey, 07054 Company: Teva ... **The opportunity** The Director Compliance & Ethics, Global R&D and Medical Affairs reports to...will leverage in-depth expertise and knowledge of the industry's legal/ regulatory environment in order to provide clear, concise and… more
    Teva Pharmaceuticals (09/07/24)
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  • Managing Director , Legal…

    New York State Energy Research and Development Aut (New York, NY)
    …senior attorney (the "MD-L&R") to join its management team, lead its Legal & Regulatory Affairs ("LRA") team and provide legal advice and strategic counsel with ... York is leading the nation in the fight on global climate change and the transition to a clean...being directly responsible for a variety of legal and regulatory affairs activities and deliverables at the… more
    New York State Energy Research and Development Aut (08/31/24)
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  • Associate Director , Regulatory

    Gilead Sciences, Inc. (Parsippany, NJ)
    Regulatory Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical ... or other special projects. May initiate and/or contribute to global process improvements. + Provides regulatory guidance...Experience working with external contractors supporting the work of regulatory affairs is a plus. + Experience… more
    Gilead Sciences, Inc. (07/02/24)
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  • Associate Director , Regulatory

    Bristol Myers Squibb (Madison, NJ)
    …more: careers.bms.com/working-with-us . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of ... + Ensure global development plans will meet global regulatory requirements by soliciting and integrating...with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience… more
    Bristol Myers Squibb (07/19/24)
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  • Medical/Scientific Director , Medical…

    AbbVie (Florham Park, NJ)
    …scientific and medical expertise to cross-functional teams, including research and development, regulatory affairs , market access, and commercial teams. + Ensure ... be determined by the qualifications listed below. The Medical/Scientific Director , Medical Affairs - Psychiatry Pipeline is...compliance with regulatory and ethical standards in all medical … more
    AbbVie (08/21/24)
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  • Associate Medical/Scientific Director

    AbbVie (Florham Park, NJ)
    …statistics, regulatory , etc) as they relate to on-going medical affairs projects. May assist as consultant/liaison with other corporations when working under ... assist with the scientific review, development, execution and communication of affiliate/area/ global medical affairs sponsored or supported clinical research… more
    AbbVie (08/30/24)
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