• Director, MEG Lead Neuroscience, Medical Evidence…

    Bristol Myers Squibb (Princeton, NJ)
    …of the organization. + In depth knowledge of overall project planning and project management of clinical trials + Proven ability to partner effectively ... industry collaborator and partner of choice. + Provide oversight of Medical clinical trials end-to-end (ie, start-up, influence governance outcomes, partner with… more
    Bristol Myers Squibb (01/18/26)
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  • Asst Dir, Quality Assur, CMSU

    University of Rochester (Rochester, NY)
    …employees, colleagues, and/or customers. + Provides compliance support for the release of clinical trial supplies to allow for timely distribution in accordance ... and expiry/retest program for all on-going studies. Interacts directly with client, Project Manager , Principal Investigators, and analytical facility to obtain… more
    University of Rochester (12/10/25)
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  • Department Program Spec I

    University of Rochester (Rochester, NY)
    …of the URCC NCORP Research Base (an NCI funded $30+ million nationwide cancer clinical trial network with more than 35 partner institutions across the country), ... PEAK activities in collaboration with the Director and PEAK Manager . Administrative Duties for RENEW Clinical Exercise...Office Suite and social media platforms required + Strong project management skills, with the ability to manage multiple… more
    University of Rochester (11/06/25)
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  • Medical Affairs Sr Scientist

    J&J Family of Companies (Irvine, CA)
    …accommodation resource. \#LI-Hybrid **Required Skills:** **Preferred Skills:** Analytical Reasoning, Clinical Trial Protocols, Data Savvy, Detail-Oriented, Drug ... for humanity. Learn more at https://www.jnj.com **Job Function:** Discovery & Pre- Clinical / Clinical Development **Job Sub** **Function:** Animal Medicine **Job… more
    J&J Family of Companies (01/13/26)
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  • Principal Scientist, In Vivo Pharmacology,…

    Bristol Myers Squibb (Cambridge, MA)
    …and patient enrichment hypotheses to enable efficient decision making in early clinical trials . We are optimally positioned to complement the world-class ... T cell engager drug discovery programs. Working closely with project teams and key stakeholders, lead the development of...perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of… more
    Bristol Myers Squibb (01/18/26)
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  • Associate Director, Program Management

    Bristol Myers Squibb (Princeton, NJ)
    …more GPTs and associates sub-teams of moderate complexity in the early/late development space. The Project Manager may also serve as part of a PM team supporting ... and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency,… more
    Bristol Myers Squibb (01/17/26)
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  • Transportation Assistant

    Veterans Affairs, Veterans Health Administration (Bonham, TX)
    Summary The incumbent works with the VTS Supervisory Mobility Manager for transportation workload forecasting, scheduling design, procedure development, and quality ... of the Veteran Transportation Services program. The incumbent must have knowledge of clinical services, related software and programs as they relate to clinical … more
    Veterans Affairs, Veterans Health Administration (01/18/26)
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  • Lead Prosthetic Clerk

    Veterans Affairs, Veterans Health Administration (Dallas, TX)
    …Service to include office management functions, budget and finance, office/ clinical support service, clinical / program analysis, document control, determining ... products and services. Articulate and communicate to the team the assignment, project , problem to be solved, actionable events, milestones, and/or program issues… more
    Veterans Affairs, Veterans Health Administration (01/17/26)
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  • Director CMC Regulatory Affairs

    Regeneron Pharmaceuticals (Troy, NY)
    …+ Successful leadership in delivering CMC/CP sections of marketing authorizations, clinical trial applications (CTA/IND), and post-approval submissions for ... role involves overseeing regulatory affairs staff, various outside contractors, supporting project teams and development partners, and leading activities with the… more
    Regeneron Pharmaceuticals (12/20/25)
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  • Assistant Director Compliance and Regulatory…

    Brown University (Providence, RI)
    …that investigators receive guidance on IRB submissions, post-approval regulatory requirements, clinical trial compliance, FDA regulations, and clinical ... and for-cause audits, in collaboration with the Quality and Compliance Manager . The Assistant Director evaluates program effectiveness by analyzing metrics,… more
    Brown University (11/21/25)
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