• Executive Director - Non-Clinical Safety…

    Organon & Co. (Jersey City, NJ)
    …cross-functional interactions with early clinical development, late-clinical development, regulatory affairs , safety and pharmacovigilance, Chemistry, ... ranging from discovery through late-stage development. This is a scientific leadership position that includes management responsibilities of the non-clinical… more
    Organon & Co. (11/18/25)
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  • US Medical Director, Dermatology (NextGen…

    Sanofi Group (Morristown, NJ)
    …medical leadership role within Sanofi's Next Gen Immunology Medical Affairs organization, driving evidence-based medical strategy in dermatology and rheumatology ... therapeutic areas. Reporting to the Senior Medical Director, Dermatology & Rheumatology, this position requires deep expertise in biologics, innovative real-world… more
    Sanofi Group (10/29/25)
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  • Head of Clinical Development

    Mallinckrodt Pharmaceuticals (Bridgewater, NJ)
    …support marketed products + Coordinates seamlessly with Clinical Operations and with Regulatory Affairs + Supervises the activities and the performance ... Job Description Summary Job Description The Head of Clinical Development is a senior member of the R&D Leadership team with responsibility for supporting the… more
    Mallinckrodt Pharmaceuticals (11/25/25)
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  • Executive Director, Global Program Lead - Next…

    Bristol Myers Squibb (Princeton, NJ)
    …Leadership organization are strategic-thinking, problem-solving, and action oriented scientific leaders who bring drug development and commercialization insights ... late-stage challenges (eg, trends in disease area therapeutic advances, and evolving regulatory , patient advocacy and market access environments) to create a vision… more
    Bristol Myers Squibb (10/18/25)
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  • Director, Medical Strategy, Global Medical…

    Bristol Myers Squibb (Princeton, NJ)
    …decks, and review scientific content and publication + Collaborates with the Senior Director and medical matrix in the development of Customer Impact Plan and ... of the US/Global medical plan. The Director will report to the Senior Director, Admilparant Medical Program Lead. **Key Responsibilities:** + Support the execution… more
    Bristol Myers Squibb (11/26/25)
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  • Principal Sterilization Microbiologist

    System One (Park Ridge, NJ)
    …+ Partner with product development, packaging, operations, quality, and regulatory affairs to integrate microbiological and sterilization requirements ... technical direction, leading high-impact sterilization programs, and ensuring full regulatory compliance across the product lifecycle-from development through commercialization.… more
    System One (09/25/25)
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  • Director, Medical Writing, Oncology (1 of 2)

    J&J Family of Companies (Titusville, NJ)
    …health for humanity. Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group **Job Sub** **Function:** Medical Writing **Job Category:** People ... will be considered as a single submission. **Purpose:** The Director of Regulatory Medical Writing (RegMW) is recognized as a leader with extensive medical… more
    J&J Family of Companies (11/18/25)
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  • Principal Scientist, Clinical Research, Immunology

    Merck (Rahway, NJ)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Clinical Director May Be… more
    Merck (11/22/25)
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  • Associate Director, Global Regulator Strategy,…

    Bristol Myers Squibb (Madison, NJ)
    …(Masters, PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** ... the regulatory strategy, issues, and risks in written and verbal format to regulatory senior leadership team and other governing bodies. + Ability to broadly… more
    Bristol Myers Squibb (11/26/25)
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  • Sr. Manager, Supply Chain

    Mitsubishi Chemical Group (Jersey City, NJ)
    …by closely working with MTP internal colleagues in various functions (Quality Assurance, Regulatory Affairs , Marketing, Market Access, Medical Affairs , Drug ... effectively with colleagues in Supply Chain, Accounting, Market Access, Quality Assurance, Regulatory Affairs , Finance, etc. of Mitsubishi Tanabe Pharma Group,… more
    Mitsubishi Chemical Group (09/24/25)
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