• Associate Clinical Project

    IQVIA (Parsippany, NJ)
    …and owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are ... to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery,… more
    IQVIA (12/18/25)
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  • Associate Director, Product…

    CenterWell (Trenton, NJ)
    …Healthcare. + Strong experience inchangemanagement strategies. + Six Sigma and/or Project Management Institute (PMI) certification. **Additional Information** + ... a part of our caring community and help us put health first** The Associate Director, Product Management Conceives of, develops, delivers, and manages products… more
    CenterWell (12/16/25)
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  • Associate Director, External…

    Regeneron Pharmaceuticals (Warren, NJ)
    …practices and processes to achieve objectives. + Exhibit strong problem-solving, analytical, and project management skills. + Thrive in a matrix environment with ... The Associate Director, External Data Services, plays a critical...and industry best practices. This position collaborates closely with Clinical Data Management teams and External Data… more
    Regeneron Pharmaceuticals (10/04/25)
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  • Associate Director, Clinical Supply…

    Bristol Myers Squibb (Madison, NJ)
    …Assure coherence between the global supply strategy, Project Team objectives and Clinical Supply Chain management objectives." + Provide overall project ... development, of the functions and processes relevant to drug development, and project management principles applicable to the biopharmaceutical environment. +… more
    Bristol Myers Squibb (12/17/25)
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  • Associate Principal Scientist,…

    Merck (Rahway, NJ)
    … Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and ... Principal Scientist can also be responsible for several effectiveness studies within a project , participating as the clinical representative in project teams… more
    Merck (12/18/25)
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  • Statistical Project Leader…

    Sanofi Group (Morristown, NJ)
    …to do advanced statistical analyses using SAS or R. + Demonstrated strong project management , interpersonal and communication skills. + Exhibited expertise to ... **Job Title:** Statistical Project Leader ( Associate Director) **Location:** Morristown,...and Decision Science (EGDS) group** at Sanofi unites Biostatistics, Clinical Statistical Modeling, and Real-World Evidence to revolutionize data-driven… more
    Sanofi Group (12/06/25)
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  • Project Leadership - Biotech…

    Parexel (Trenton, NJ)
    …patients we serve. Parexel's defined Biotech Division offers opportunities for seasoned Project Management professionals with a strong background running global ... minimum, 2+ years' experience leading Global Clinal Trials in Project Management within a CRO (preferred), Biotech...be required for the more senior roles of Senior Project Leader, Associate Project Director,… more
    Parexel (12/28/25)
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  • Senior Clinical Research Associate

    Parexel (Trenton, NJ)
    Clinical Research Associate (Sr. CRA) is responsible for the site management , site monitoring and close-out of assigned clinical trials investigator sites ... documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management , study progress and metrics + Identify… more
    Parexel (12/07/25)
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  • Associate Medical Director, Clinical

    Sumitomo Pharma (Trenton, NJ)
    …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The ... associate medical director is responsible for the leadership, development, and management of clinical studies while building and maintaining relationships… more
    Sumitomo Pharma (11/15/25)
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  • Sr. Clinical Research Associate

    Parexel (Trenton, NJ)
    Clinical Research Associate (Sr. CRA) is responsible for the site management , site monitoring and close-out of assigned clinical trials investigator sites ... documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management , study progress and metrics + Identify… more
    Parexel (12/11/25)
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