• Lead Compliance Specialist

    J&J Family of Companies (Raritan, NJ)
    …https://www.jnj.com **Job Function:** R&D Operations **Job Sub** **Function:** Clinical Trial Project Management **Job Category:** Professional **All Job Posting ... activities: + Conducting compliance monitoring visits. + Performing assigned reviews of Trial Master File, training compliance documentation and other checks per CRM… more
    J&J Family of Companies (08/08/25)
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  • Paralegal

    American Water (Camden, NJ)
    …the proceeding to provide feedback to the attorney * Solid knowledge of litigation support and case management, including trial preparation * Draft and negotiate ... responses with in-house and outside counsel * Familiarity with litigation support duties at both the trial and appellate level in state and federal courts * Key… more
    American Water (08/01/25)
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  • Regional Medical Scientific Director (Medical…

    Merck (Trenton, NJ)
    …Scientific Director is aligned to: Scientific Exchange, Research, Scientific Congress Support , and Scientific Insights. + Regional Medical Scientific Director liaise ... on-boarding and/or sharing of therapeutic expertise. + This position will support our company's Rheumatology and Dermatology Immunology program + The position… more
    Merck (07/31/25)
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  • Associate Director, Quantitative Pharmacology…

    Merck (Rahway, NJ)
    …Rahway, NJ is seeking a curious and collaborative Associate Director to support our rapidly expanding cardiometabolic and ophthalmology pipelines. As an Associate ... a quantitative drug developer taking advantage of our end-to-end pipeline support in one of the world's most research-intensive biopharmaceutical companies.… more
    Merck (08/08/25)
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  • Senior Statistical Programmer- Analysis…

    Merck (Rahway, NJ)
    …Ensure programmatic traceability from data source to analysis/modeling result + Support the development of programming standards to enable efficient and high-quality ... of programming deliverables + Provide technical consultation and analytical support to early development statisticians for exploratory and unplanned statistical… more
    Merck (07/31/25)
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  • Scientific/Medical Director, Medical Affairs…

    AbbVie (Florham Park, NJ)
    …strategic medical input into core brand (product) strategies, and to support medical affairs, marketing activities (promotional material generation and product ... 4+ years of experience is preferred. + Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials… more
    AbbVie (07/26/25)
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  • Principal Scientist, Biostatistics

    Merck (Rahway, NJ)
    …a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase II/ III trials. The knowledge must be sufficient ... statistical methods applied to designing and analyzing clinical trials in support of worldwide regulatory submissions. This position involves interaction with… more
    Merck (07/16/25)
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  • Oncology Clinical Research Nurse

    Vitalief (New Brunswick, NJ)
    …Nurse to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our mission and our clients' mission to impact and save lives. This ... Activation office to initiate and activate all new clinical trial protocols assigned utilizing Oncore Study-start up task list....or clinic setting. + Experience working in a clinical research/ trial participant facing role is a big plus (but… more
    Vitalief (08/10/25)
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  • Global Study Data Leader

    Sanofi Group (Morristown, NJ)
    …and applicable regulatory guidance. Provide comprehensive data management expertise and support to team members. Coordinate cross functional teams globally to ensure ... the flawless conduct of a clinical trial . Ensure activities are completed according to agreed standards...scope and objectives. . Solid knowledge of the clinical trial development process and understanding of relevant and current… more
    Sanofi Group (08/10/25)
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  • Senior Scientist, Statistical Programming

    Merck (Rahway, NJ)
    …+ Ensure programmatic traceability from data source to analysis/modeling result. Support the development of programming standards to enable efficient and ... plus 3 years SAS programming experience in a clinical trial environment OR a Bachelor's degree in Computer Science,...plus 5 years SAS programming experience in a clinical trial environment. **Minimum requirement:** + Must have experience in… more
    Merck (07/23/25)
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