• Senior Director , Global

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …ensuring appropriateness throughout the product's lifecycle and across different indications. + Represent Global Regulatory Affairs on the GPT ( Global ... responsible for providing oversight and formulation of strategy for global regulatory submissions in Oncology in the...pharmaceutical industry + 7 or more years with direct regulatory affairs experience + Experience in … more
    Daiichi Sankyo Inc. (08/22/24)
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  • Director , Global Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …diseases and immune disorders. **Summary** Responsible for leading and developing global regulatory strategy for assigned development projects. Represents ... global strategy. + Responsible for ensuring aligned global regulatory strategy is endorsed by GPT...relevant pharmaceutical experience including 5 years of experience within Regulatory Affairs + Knowledge of IND, NDA/BLA… more
    Daiichi Sankyo Inc. (07/08/24)
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  • Associate Director , Global

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …disorders. Summary This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational ... leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). This position may...experience required + 4 or More Years of direct regulatory affairs experience, including US labeling experience… more
    Daiichi Sankyo Inc. (07/01/24)
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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 (09/12/24)
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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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  • Director , Regulatory Affairs

    Regeneron Pharmaceuticals (Tarrytown, NY)
    The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus ... on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. We are a hands-on culture so responsibilities will include… more
    Regeneron Pharmaceuticals (09/11/24)
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  • Director , US Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …or More Years in the pharmaceutical industry required. + 8 or More Years in regulatory affairs + Experience in providing regulatory strategic input into the ... preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that regulatory more
    Daiichi Sankyo Inc. (09/02/24)
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  • Associate Director , US Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …More Years in the pharmaceutical industry preferred + 1 or More Years in regulatory affairs required + Experience in (s)NDA/BLA filing to FDA preferred ... preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that regulatory more
    Daiichi Sankyo Inc. (06/19/24)
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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 (09/12/24)
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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 (09/12/24)
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  • Medical/Scientific Director , Medical…

    AbbVie (Florham Park, NJ)
    …understanding of relevant therapeutic area required. + 7-10 years of experience in Medical Affairs with Global Medical Affairs experience highly preferred. + ... and scientific strategic and operational input into core medical affairs activities such as: healthcare professional/provider interactions (HCPs, Patients and… more
    AbbVie (09/12/24)
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  • Scientific Director , Medical…

    AbbVie (Florham Park, NJ)
    …can sit in our Lake County, IL or Madison, NJ offices. The Scientific Director for US Medical Affairs in CNS/Psychiatry provides specialist medical and ... with the scientific review, development, approval, execution, and communication of affiliate/area/ global medical affairs sponsored or supported clinical research… more
    AbbVie (09/12/24)
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  • Director , US Medical Affairs

    Bristol Myers Squibb (Madison, NJ)
    …**Key Responsibilities** + Strategic and Tactical Planning: Responsible for the US Medical Affairs plans, in coordination with the Global Medical Affairs ... and in their personal lives. Read more: careers.bms.com/working-with-us . The Medical Director , US Medical, Multiple Myeloma will report to the Senior Director more
    Bristol Myers Squibb (08/30/24)
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