• Senior Manager, Global Regulatory Affairs

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …(eg, clinical development, project management, quality assurance, etc.) in pharmaceutical or healthcare related industry. Experience with FDA or other health ... Skills, and Competencies** **K** **nowledge** - Experience working in the pharmaceutical and/or healthcare industry. - Knowledge and experience with preparation of… more
    Otsuka America Pharmaceutical Inc. (08/22/25)
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  • Labeling Associate - Regulatory Affairs

    Robert Half Office Team (Bridgewater, NJ)
    …to regulatory compliance and process improvement within the health and pharmaceutical industry. The ideal candidate will support labeling projects, facilitate ... leaders to enhance understanding of process needs and objectives. * Represent Clinical Development Operations in project management meetings to provide insights and… more
    Robert Half Office Team (08/08/25)
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  • Associate Director, Marketing Analytics - Women's…

    Sumitomo Pharma (Trenton, NJ)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... and prioritize key business questions with the cross-functional support of medical, clinical , brand teams, and other partners in the organization. + Manage… more
    Sumitomo Pharma (07/18/25)
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  • Sr. Scientist, Statistical Programming- PKPD…

    Merck (Rahway, NJ)
    …data in a variety of formats with minimal requirements, knowledge of pharmaceutical development processes + Efficiently manipulates clinical trial datasets ... or related field plus 5-9 years SAS programming experience in a clinical trial environment + MS in Computer Science, Statistics, Applied Mathematics, Life… more
    Merck (08/26/25)
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  • Oncology Regional Medical Scientific Associate…

    Merck (Trenton, NJ)
    …policies. + Maintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI) for the RMSD's ... retention efforts to achieve study milestones + Upon request from Global Clinical Trial Operations (GCTO), + Recommends study sites and identifies potential… more
    Merck (08/23/25)
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  • Program Analyst - Remote

    Prime Therapeutics (Trenton, NJ)
    Clinical Program Management, Utilization Management (UM), Formulary, GuidedHealth, Pharmaceutical Trade Relations, Pharmacy Audit, Clinical Operations and/or ... Utilization Review (DUR), Concurrent DUR, member eligibility information, pharmacy and/or pharmaceutical performance and analytics and other reports as needed +… more
    Prime Therapeutics (09/03/25)
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  • Associate Director, Global Labeling Product Leader

    J&J Family of Companies (Raritan, NJ)
    …Entity (NME) submissions is preferred. + Relevant experience in the pharmaceutical industry (eg, Regulatory Affairs, Clinical , Medical Information, ... partner with Global Regulatory Leads (GRLs) and other functional area partners ( clinical , safety, market access, commercial, medical affairs) to ensure the global… more
    J&J Family of Companies (08/29/25)
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  • Account Manager, Non-Pharma

    IQVIA (Parsippany, NJ)
    …clients who require deep healthcare insights but do not own pharmaceutical products. This unique segment supports a diverse portfolio of organizations-including ... data into actionable intelligence for clients operating outside the traditional pharmaceutical landscape. Joining this team means being part of a collaborative,… more
    IQVIA (08/27/25)
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  • Manager, PVRM

    Sumitomo Pharma (Trenton, NJ)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... across the SMPA organization including, but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data Management and… more
    Sumitomo Pharma (08/01/25)
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  • Medical Director, Global Medical Affairs, Early…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …Collaborate closely with other key functions, including regional medical leads, clinical development, global value and real-world evidence, US and global commercial ... development (phase 1) assets either within Medical Affairs, Regulatory Affairs, or Clinical Development is preferred. + Minimum of 7+ years of relevant experience… more
    Otsuka America Pharmaceutical Inc. (07/16/25)
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