• Vice Chair of Research, Department of Emergency…

    Geisinger (Wilkes-Barre, PA)
    …million in external grant and contract revenue, >1,400 active research projects, including clinical trials , and >1,090 publications. The Vice Chair of Research ... an Emergency Medicine physician with a proven record in clinical research to join our team as the Vice...and includes the support of a dedicated full-time Research Project Manager who assists in advancing the… more
    Geisinger (11/11/25)
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  • Summer Intern - BioAnalytical Sciences

    Genentech (South San Francisco, CA)
    …are measured in patient blood or other biological samples collected during a clinical trial ? Bioanalytical assays specifically measure the protein drug molecule ... industry. BAS has several groups working on preclinical and clinical programs developing bioanalytical assays with a variety of...Francisco, on-site.** **The Opportunity** + You will lead a project over the course of 12 weeks under the… more
    Genentech (11/26/25)
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  • Senior Director, Program Management Systems…

    Bristol Myers Squibb (Princeton, NJ)
    …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... Director oversees key platforms-including ePlan (Planisware) for the development plan per project , Microsoft Project / Planner for bottom-up planning of… more
    Bristol Myers Squibb (11/16/25)
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  • Formulation Associate

    Reckitt (Salt Lake City, UT)
    …we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier ... the product development process + Work cross-functionally and lead project teams to achieve key milestones and objectives +...with any issues or risks clearly highlighted to line manager in a timely manner. + Prepare relevant product… more
    Reckitt (10/25/25)
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  • Principal Statistical Programmer

    Regeneron Pharmaceuticals (Warren, NJ)
    …study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports. If ... study team on all programming matters according to the project strategies. **In this role, a typical day might... leadership and programming support for processing data from clinical studies. Requirements will be identified according to a… more
    Regeneron Pharmaceuticals (10/29/25)
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  • Data Ambassador

    ICON Clinical Research (Cambridge, MA)
    …mission to shape the future of clinical development. We are currently seeking a Project Manager , Laboratory to join our diverse and dynamic team. As a ... Project Manager , Laboratory at ICON, you will...Project Manager , Laboratory at ICON, you will play a pivotal...will play a pivotal role in designing and analyzing clinical trials , interpreting complex medical data, and… more
    ICON Clinical Research (10/07/25)
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  • Director Drug Development Program Management

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …management with knowledge of the drug development process as well as understanding of clinical trials . \#hematology Does this sound like you? Apply now to take ... leadership, direction and support to a team, program or project of moderate to large scope, [within a given...performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron's on-site policy and… more
    Regeneron Pharmaceuticals (10/29/25)
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  • Transportation Assistant

    Veterans Affairs, Veterans Health Administration (Tucson, AZ)
    …works with the Veteran Transportation Service (VTS) Supervisory Mobility Manager for transportation workload forecasting, scheduling design, procedure development, ... responsibilities; (3) Program Support responsibilities. The incumbent must have knowledge of clinical services, related software, and programs as they relate to … more
    Veterans Affairs, Veterans Health Administration (11/25/25)
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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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  • 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 (11/13/25)
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