• Principal Product Software Engineer AI | Legal…

    Wolters Kluwer (Princeton, NJ)
    …to help save lives, improve how we do business, and build better judicial and regulatory systems. We help them get it right. This role is part of the Advanced ... we support, VitalLaw, is trusted by customers to help legal professionals achieve regulatory compliance and better understand complex legal issues in key areas like… more
    Wolters Kluwer (09/27/25)
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  • Vice President, Regulatory Affairs…

    Sumitomo Pharma (Trenton, NJ)
    …a diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For ... HTA submissions. The individual will be responsible for leading development of all non-clinical and clinical regulatory ...the Marketing Brand Teams, Legal, Medical Affairs and Clinical Research in the development of advertising and… more
    Sumitomo Pharma (09/23/25)
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  • VP, Regulatory Affairs R&D Biopharma

    Sumitomo Pharma (Trenton, NJ)
    …a diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For ... making on all Regulatory matters in close partnership with the Chief Development Officer and other key stakeholders + Establish key business metrics with market… more
    Sumitomo Pharma (09/10/25)
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  • Senior Principal Scientist, Clinical…

    Merck (Rahway, NJ)
    …study reports, or publication; and + Participation in internal and joint internal/external research project teams relevant to the development of new compounds ... regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director in ensuring that appropriate… more
    Merck (10/01/25)
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  • Executive Director, Regulatory CMC Small…

    Merck (Rahway, NJ)
    Regulatory Compliance Audits, Regulatory Requirements, Regulatory Strategy Development , Research Development , Risk Analysis {+ 1 more} **Preferred ... Regulatory Affairs CMC (Global Regulatory Affairs & Clinical Safety), Research and Development (R&D), Manufacturing, and Global Human Health (GHH)… more
    Merck (10/01/25)
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  • Senior Principal Scientist, Clinical…

    Merck (Rahway, NJ)
    Development , Pulmonary Arterial Hypertension, Pulmonary Disease Research , Pulmonary Disease Treatment, Pulmonary Disorders, Pulmonology, Regulatory ... development , including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director may… more
    Merck (09/22/25)
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  • Director, Global Regulatory Affairs…

    Sanofi Group (Morristown, NJ)
    …The Director plays an active role in shaping labeling strategy early in product development by providing regulatory input into clinical development plans, ... consistency of labeling content across global markets and supports interactions with regulatory authorities during labeling development and negotiation. We are… more
    Sanofi Group (10/02/25)
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  • Director, Early Precision Medicine…

    Bristol Myers Squibb (Princeton, NJ)
    …risk mitigation planning. + Cultivate inclusive, high-impact collaboration with Precision Medicine, Research teams, Global and Regional Regulatory Leads, Global ... Provide regulatory support on product partnership, vendor management and business development opportunities + Serve as a strategic regulatory thought leader… more
    Bristol Myers Squibb (09/26/25)
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  • Associate Director, Regulatory Affairs

    United Therapeutics (Trenton, NJ)
    …perfusion decellularization and recellularization technology, we are the world leader in the research and development of fully biologic organs. Our approach is ... spectrum of donor needs. We are focused on the research and development of transplantable kidneys (...of study or 7+ years of biologic or pharma regulatory experience with a PhD in life… more
    United Therapeutics (09/27/25)
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  • Senior Director, Clinical Research

    Merck (Rahway, NJ)
    development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May Be ... study reports, or publication + Participation in internal and joint internal/external research project teams relevant to the development of new compounds,… more
    Merck (09/22/25)
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