• Lead Clinical Research Associate

    Oracle (Sacramento, CA)
    …quality visits:** Be available to travel to clinical sites to train and monitor site activities as needed. While there is no guaranteed travel, flexibility ... Be available to travel to clinical sites to train and monitor site activities as needed. While there is no guaranteed travel, flexibility is required.… more
    Oracle (01/17/26)
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  • Oversight Monitor

    Actalent (Los Angeles, CA)
    …to door Job Title: Oversight Monitor Job Description The Oversight Monitor provides independent oversight of clinical monitoring activities conducted by ... position focuses on evaluating the quality, consistency, and adequacy of site monitoring, issue management, and documentation practices to ensure trial integrity,… more
    Actalent (01/15/26)
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  • Session Monitor

    System One (Redding, CA)
    …patient interaction and support + Provide client-facing leadership during feasibility, site preparation, and trials + Administer clinical assessments directly ... Job Title: Licensed Session Monitor / Dosing Facilitator Location: Redding, CA-Onsite Hours:...work at the ground level for a new psychedelic-focused site in Redding, CA. Initial work will be ad… more
    System One (12/26/25)
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  • Assistant Session Monitor

    System One (Redding, CA)
    Monitor / Lead Psychiatrist during psychedelic dosing sessions at our client's Clinical Research site in Redding, CA. This role involves direct patient ... Job Title: Assistant Session Monitor Location: Redding, California Type: Ad-hoc Contract Compensation:...activities + Ensure adherence to study protocols and Good Clinical Practice (GCP) standards + Document observations and assist… more
    System One (12/26/25)
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  • Sr. Clinical Research Associate - Oncology…

    Parexel (Sacramento, CA)
    …database release as needed + May undertake the responsibilities of an unblinded monitor where appropriate ** Clinical /Scientific and Site Monitoring Risk:** + ... CRA) is responsible for the site management, site monitoring and close-out of assigned clinical ...(SOPs) and commensurate with emerging issues and technologies + Monitor site level adverse events (AEs) and… more
    Parexel (12/11/25)
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  • Senior Clinical Research Associate/…

    Parexel (Sacramento, CA)
    …database release as needed + May undertake the responsibilities of an unblinded monitor where appropriate ** Clinical /Scientific and Site Monitoring Risk** + ... (SOPs) and commensurate with emerging issues and technologies + Monitor site level adverse events (AEs) and...checks, when applicable **Collaboration** + Reports to Director of Clinical Site Operations (DCSO) or Director of… more
    Parexel (12/07/25)
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  • Clinical Research Coordinator 2

    Stanford University (Stanford, CA)
    Clinical Research Coordinator 2 **School of Medicine, Stanford, California, United States** Research Post Date 3 days ago Requisition # 107839 Stanford University is ... seeking a Clinical Research Coordinator 2 to conduct clinical ...passionately care, to advance our ability to understand, diagnose, monitor and ultimately to cure disease or to prevent… more
    Stanford University (12/03/25)
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  • Sr. Clinical Research Program Manager

    Stanford University (Stanford, CA)
    …of consent forms for approval by Human Subjects Panel for investigator-initiated multi- site clinical research trials including behavioral and social needs ... ability to implement, organize and perform oversights of all aspects of complex, multi- site , multi-level clinical studies combined with knowledge of good … more
    Stanford University (01/10/26)
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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 (12/19/25)
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  • Lead Clinical Research Associate

    University of Southern California (San Diego, CA)
    … Monitoring Team at study specific meetings. Provide study updates on Clinical Monitoring team metrics, site escalations, and other monitoring efforts. ... with study CRAs to meet study milestones. + Review Monitor Visit Reports (MVR) and provide feedback to team....+ Conduct onsite and remote monitoring visits for assigned clinical sites. Review Investigator Site Files, study… more
    University of Southern California (01/08/26)
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