• Clinical Monitor Line Manager

    University of Southern California (San Diego, CA)
    …and investigator initiated clinical research + Responsible for managing study site assignments, daily operations, monitor metrics reviews, and data query ... Clinical Monitor Line ManagerApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/San-Diego-CA/ Clinical...placements, and closures + Ensures site qualifications, initiations, monitoring, and study closeout visits are… more
    University of Southern California (08/29/25)
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  • Director, Early Clinical Development…

    Bristol Myers Squibb (Brisbane, CA)
    …**Position Responsibilities** **Medical Monitoring** + Serves as an independent Medical Monitor for clinical trials from Phase 1 through Proof-of-Concept ... and medical accountability for multiple trials across early development clinical lifecycle + Manages site interactions in...across early development clinical lifecycle + Manages site interactions in partnership with the Clinical … more
    Bristol Myers Squibb (08/12/25)
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  • Senior Clinical Research Associate

    BeOne Medicines (Emeryville, CA)
    **General Description:** The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ... with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to… more
    BeOne Medicines (07/23/25)
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  • Director, Clinical Operations

    Bausch + Lomb (Sacramento, CA)
    …are met. + Responsible for the appropriate communication with and maintenance of clinical study sites including training of site personnel in the study ... and lock process. + Liaise with vendors and study site personnel and clinical investigators to provide...external vendors. + Ensure subordinates and vendors manage and monitor study related expenses to meet forecast. Regulatory Reports:… more
    Bausch + Lomb (06/07/25)
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  • Clinical Research Associate

    University of Southern California (San Diego, CA)
    …+ Thorough understanding of study protocol and manuals. + Work closely with Lead Clinical Monitor /Lead CRA to escalate site compliance issues. + Participate ... not limited to: + Conduct onsite and remote monitoring for assigned clinical sites and co- monitor visits. Review Investigator Site Files, study data, perform… more
    University of Southern California (06/11/25)
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  • Clinical Research Coordinator Associate (1…

    Stanford University (Stanford, CA)
    …of clinical studies, consent patients in person, interview patients, monitor follow-up, coordinate collection of clinical data and research samples ... Clinical Research Coordinator Associate (1 Year Fixed-Term) **School...are completed. + Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and… more
    Stanford University (08/07/25)
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  • Clinical Research Coordinator 2

    Stanford University (Stanford, CA)
    Clinical Research Coordinator 2 **School of Medicine, Redwood City, California, United States** Research Post Date Aug 18, 2025 Requisition # 107076 The Department ... of Orthopaedic Surgery is seeking a Clinical Research Coordinator 2 (CRC2) to conduct ...Develop and manage systems to organize, collect, report, and monitor data collection. Extract, analyze, and interpret data. +… more
    Stanford University (08/19/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Jun 10, 2025 Requisition # 106623 The ... Clinical Research Coordinator Associate is responsible for the overall...are completed. + Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and… more
    Stanford University (08/07/25)
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  • Senior Clinical & Population Health Analyst

    Highmark Health (Sacramento, CA)
    …and leads the design, development, execution, dissemination and interpretation of clinical and population health analyses, metrics and reports using clinical ... , member, financial and administrative data to identify, develop and/or monitor actionable opportunities for improving health and healthcare outcomes and clinical… more
    Highmark Health (07/22/25)
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  • Clinical Research Associate - IMM/Cross TA…

    ICON Clinical Research (Los Angeles, CA)
    …and track site staff training and maintain compliance records + Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting + Support subject ... site progress and escalate risks or issues to the clinical team + Assist in tracking site budgets and ensuring timely site payments (as applicable) +… more
    ICON Clinical Research (08/28/25)
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