• Research Administrator 2 (Remote Eligible)

    Stanford University (Stanford, CA)
    …status. **In this role, you will** **:** + Participate with principal investigator in the preparation of the administrative components of proposals within parameters ... Serve as a subject matter expert and overall technical resource to principal investigator and other university staff. + Participate in and contribute to process… more
    Stanford University (12/04/25)
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  • Senior Clinical Research Associate - West Coast…

    Parexel (Sacramento, CA)
    …data from study sites as per required timelines. + Manages study supplies ( Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site. ... visit reports in CTMS and provides timely feedback to the Principal Investigator , including follow-up letter, within required timelines and in line with Client… more
    Parexel (12/03/25)
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  • Associate Clinical Research Specialist

    Kelly Services (Irvine, CA)
    …study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports), and applicable trial registration on ... Assists the clinical study team in overseeing the development and execution of Investigator agreements and trial payments + Assists in clinical data review to… more
    Kelly Services (12/03/25)
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  • Research Nurse 2

    Stanford University (Stanford, CA)
    …funds, personnel, and equipment as needed. Coordinate and collaborate with principal investigator to review study protocol and assess and analyze feasibility, budget ... * Supervise RN1s and non-clinical research staff as needed * Support sponsor investigator research. * - Other duties may also be assigned DESIRED QUALIFICATIONS: *… more
    Stanford University (12/02/25)
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  • ExploR&D Clinical Program Lead

    Lilly (San Francisco, CA)
    …+ Provide and critically evaluate content within critical documents (eg, Investigator Brochures, Risk Profiles, Study Protocols, Study Reports, Regulatory and ... Ethical filings and updates, Investigator updates, etc.). + Serve as the ExploR&D scientific leader responsible for rationale, integration of cross-functional data,… more
    Lilly (11/28/25)
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  • Postdoctoral Scientist - Stripp/Yao Labs…

    Cedars-Sinai (Los Angeles, CA)
    …but in close cooperation and in consultation with the Principal Investigator and other Research Scientists, the Postdoctoral Scientist will perform routine ... records and documentation, and analyze the results with the Principal Investigator . + Analyzes, interprets, summarizes, and compiles data. + Operates and… more
    Cedars-Sinai (11/28/25)
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  • Medical Science Liaison - Oncology (North West)

    Sumitomo Pharma (San Francisco, CA)
    …in drug/brand development. Identify, initiate, coordinate, evaluate and monitor investigator -sponsored studies intended to support the clinical and scientific ... products. Help develop and manage timelines of publication plans of investigator -sponsored studies. Assist in the identification, evaluation, and engagement of… more
    Sumitomo Pharma (11/27/25)
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  • Clinical Research Coordinator - Urology

    UCLA Health (Los Angeles, CA)
    …multicenter clinical trials (both NIH and industry-sponsored), local investigator -initiated clinical trials, and/or programmatic clinical research activities. The ... (GCP). The Clinical Research Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors,… more
    UCLA Health (11/27/25)
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  • Clinical Research Coordinator 2

    Stanford University (Stanford, CA)
    …define best practices. + Develop study budget with staff and principal investigator , identifying standard of care versus study procedures. Track patient and study ... study document to ensure ongoing regulatory compliance. + Work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA… more
    Stanford University (11/26/25)
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  • Senior Site Manager

    Kelly Services (Irvine, CA)
    …study protocol, informed + consents, CRF, monitoring plan, study manual, investigator brochure, annual reports, ) + Ensure registration on www.clinicaltrials.gov ... and company + personnel + Oversee the development and execution of Investigator agreements and trial payments + Responsible for clinical data review to… more
    Kelly Services (11/26/25)
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