• Clinical Research Coordinator II

    Stanford University (Stanford, CA)
    compliance . Regularly inspect study document to ensure ongoing regulatory compliance . + Work with principal investigator to ensure Investigational New ... work. + Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing… more
    Stanford University (10/03/25)
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  • Clinical Research Coordinator 2 (Fixed-term 24…

    Stanford University (Stanford, CA)
    compliance . Regularly inspect study document to ensure ongoing regulatory compliance . + Work with principal investigator to ensure Investigational New ... work. + Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing… more
    Stanford University (10/03/25)
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  • Research Administrator 2

    Stanford University (Stanford, CA)
    …both routine and complex. **Duties include:** + Participate with principal investigator in the preparation of the administrative components of proposals within ... submission process, both paper and electronic; review documents for completeness and compliance . + Develop, prepare, and finalize project budgets, and provide budget… more
    Stanford University (10/03/25)
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  • Medical Director, Radiopharmaceutical Imaging…

    Bristol Myers Squibb (San Diego, CA)
    …of radiopharmaceutical imaging agents. + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial ... and regulatory documents + Conduct investigator meetings and lead site qualification and initiation visits...ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines + Establish and maintain… more
    Bristol Myers Squibb (11/26/25)
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  • Clinical Research Coordinator

    Actalent (Palo Alto, CA)
    …develop flow sheets, and complete study documents/case report forms. + Ensure compliance with research protocols and review/audit case report forms for accuracy with ... with finance and management staff. + Interact regularly with the principal investigator to ensure patient safety and adherence to proper study conduct. +… more
    Actalent (11/24/25)
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  • Clinical Development Lead Prostate (Acp3)

    Bristol Myers Squibb (San Diego, CA)
    …to design and implement clinical studies + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and ... regulatory documents + Conduct investigator meetings and lead site qualification and initiation visits...ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines + Establish and maintain… more
    Bristol Myers Squibb (11/19/25)
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  • Clinical Research Coordinator

    Actalent (Palo Alto, CA)
    …develop flow sheets, and complete study documents/case report forms. + Ensure compliance with research protocols and review and audit case report forms for ... and/or management staff. + Interact regularly with the principal investigator to ensure patient safety and adherence to proper...capture (EDC) systems. Work Environment This role offers a hybrid work environment, requiring 4 days on-site with 1… more
    Actalent (11/13/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …clinical studies and work under close direction of the principal investigator and/or study coordinator/supervisor. **Duties include:** + Serve as primary contact ... other study related documents, and complete study documents/case report forms. + Ensure compliance with research protocols and review and audit case report forms for… more
    Stanford University (10/24/25)
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  • Clinical Site Manager - Clinical Research Monitor…

    Astellas Pharma (San Diego, CA)
    …CSM is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good ... in site feasibility and/or pre-trial site assessment visits. + Attends/participates in investigator meetings as needed. + May serve as Lead CSM for specific… more
    Astellas Pharma (10/02/25)
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  • Research Administrator

    University of Southern California (Los Angeles, CA)
    …Sciences, Keck School of Medicine of USC Location: Health Sciences Campus ( Hybrid ) Position Summary:The Department of Psychiatry and the Behavioral Sciences at the ... Manage financial aspects of clinical trials, including budget tracking, investigator payments, invoices, and financial reporting for sponsors. + Proposal… more
    University of Southern California (11/19/25)
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