• Senior Manager/Associate Director,…

    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 ... United States of America **Job Description:** **Senior Manager/Associate Director, Regulatory Medical Writing X-TA** At Johnson & Johnson Innovative Medicine,… more
    J&J Family of Companies (08/16/25)
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  • Senior Principal Scientist, Clinical

    Merck (Rahway, NJ)
    …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... Development, Ethical Standards, Intellectual Curiosity, Management Process, Medical Research, Regulatory Affairs Compliance, Regulatory Reporting,… more
    Merck (09/04/25)
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  • Senior Principal Scientist, Clinical

    Merck (Rahway, NJ)
    …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects + ... Pulmonary Disease Research, Pulmonary Disease Treatment, Pulmonary Disorders, Pulmonology, Regulatory Affairs Compliance, Regulatory Compliance, Scientific… more
    Merck (08/20/25)
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  • Senior Clinical Director, Oncology Early…

    Merck (Rahway, NJ)
    …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... Management Process, Medical Research, Mentorship, Plan of Action and Milestones (POA&M), Regulatory Affairs Compliance, Regulatory Compliance {+ 5 more}… more
    Merck (08/12/25)
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  • Senior Principal Scientist, Translational…

    Merck (Rahway, NJ)
    …scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations) ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research… more
    Merck (09/03/25)
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  • Clinical Research Director - RBD

    Sanofi Group (Morristown, NJ)
    regulatory , statistics, and PM) + The CRD will lead the preparation of clinical documents/reports for regulatory submission and will attend meetings with ... **Job Title:** Clinical Research Director - RBD **Location:** Cambridge, MA...will work in conjunction with the Commercial and Medical Affairs to support the creation of the product value… more
    Sanofi Group (08/25/25)
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  • Senior Director, Clinical Research,…

    Merck (Rahway, NJ)
    …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
    Merck (09/04/25)
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  • Clinical Outcome Assessment (COA) Lead

    Sanofi Group (Morristown, NJ)
    **Job Title:** Clinical Outcome Assessment (COA) Lead **Grade:** L3 **Hiring Manager:** Benoit Arnould **Location** : Cambridge, MA or Morristown, NJ (Hybrid policy ... be critical in helping our teams accelerate progress. The remit of the Clinical Outcome Assessment (COA) team at Sanofi is to incorporate the patients' perspective… more
    Sanofi Group (09/03/25)
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  • Risk Safety Manager, Full Time, Mt.

    Virtua Health (Mount Holly, NJ)
    …will work collaboratively with key team members, Clinical Quality/Safety, Medical Affairs , and Regulatory Affairs departments in facilitating safety ... reliability principles and standardization on Cause Analysis methodology. + Partners with clinical quality team to ensure patient safety goals are met and addressed.… more
    Virtua Health (08/08/25)
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  • Manager, PVRM

    Sumitomo Pharma (Trenton, NJ)
    …but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs , Data Management and Biostatistics is essential. **Job ... as required. + Coordinate responses to ad hoc safety issues such as regulatory authority, site, or health care professional requests, along with PV physician,… more
    Sumitomo Pharma (08/01/25)
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