• Sr. Specialist , Project Management…

    Merck (West Point, PA)
    …Management Section of the GCS Planning organization. Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) creates strategic ... are not limited to:** - Participates on the Clinical Trial Team (CTT) and collaborates closely with other functional...manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair… more
    Merck (10/23/25)
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  • Sr. Specialist , Clinical Supplies Project…

    Merck (West Point, PA)
    …within the business. Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs strategic and operational plans for all activities ... as the GCS spokesperson at clinical development related meetings (ie, Clinical Trial Teams) and product development related meetings. The incumbent must have… more
    Merck (10/23/25)
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  • Associate / Medical Director - Rheumatology…

    Parexel (Harrisburg, PA)
    …appropriate for the MD + Providing risk assessment of clinical trials for local sponsorship as needed with the support of the designated Senior Medical Director/ ... assigned studies and propose /execute remediation plan in coordination with line manager and Project Leader in case of client dissatisfaction Business Development… more
    Parexel (10/11/25)
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  • Clinical Research Coordinator A/B

    University of Pennsylvania (Philadelphia, PA)
    …and may require working off site and flexible hours. Assist the regulatory specialist in preparing for all local and Central Institutional Review Board ... companies and clinical research organizations (CROs). Assist with creation of master trial file and obtain the appropriate signatures for the regulatory forms. The… more
    University of Pennsylvania (10/07/25)
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  • Clinical Research Coordinator A/B/C

    University of Pennsylvania (Philadelphia, PA)
    …such as: Assist in development of study documents. Work with Regulatory Specialist for regulatory submissions. Communicate with study team members. Recruit, consent, ... duties above with more limited supervision from the project manager . In addition, will develop complex documents such as...timelines and goals are met. Independently move a clinical trial through each phase of development, resolving issues and… more
    University of Pennsylvania (10/02/25)
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