• Senior Director, Clinical Operations Lead, Biotech…

    BeOne Medicines (San Mateo, CA)
    …Unit at regional and global level and ensure timely, quality, and efficient study planning and execution of associated clinical programs/ studies + Conduct ... accountable for the planning, budget, and oversight the execution of clinical studies of BTU assets, through partnering with execution units, that ensures clinical… more
    BeOne Medicines (11/08/25)
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  • Assistant Clinical Research Coordinator

    Stanford University (Stanford, CA)
    …Coordinator toconduct clinical research in the Stanford Child Wellness Laboratory. Studies include enrollment of healthy and critically ill children, interaction ... . Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews… more
    Stanford University (01/16/26)
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  • Principal Statistical Programmer FSP - RWD/EPI

    Cytel (Sacramento, CA)
    …EHR) + Liaise with data vendors to obtain relevant data extracts for research studies consistent with study protocols + Create analytical databases from data ... and reporting of observational data + Supporting Medical Affairs (eg observational studies leveraging RWD); Global Patient Safety and Risk Management (eg, analysis… more
    Cytel (01/14/26)
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  • Research Associate

    Parexel (Glendale, CA)
    …do after training is completed** (including but not limited): + You will understand study protocols and be able to complete required medical procedures. + Recruit ... study participants by calling the database, attending company sponsored...schools, senior centers, supermarkets, and other establishments. + Enter study participants in the study participant tracking… more
    Parexel (01/09/26)
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  • Certified Phlebotomy Technician (Per Diem)

    Parexel (Glendale, CA)
    …do after training is completed** (including but not limited): + You will understand study protocols and be able to complete required medical procedures. + Recruit ... study participants by calling the database, attending company sponsored...schools, senior centers, supermarkets, and other establishments. + Enter study participants in the study participant tracking… more
    Parexel (01/08/26)
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  • Senior Clinical Research Associate

    BeOne Medicines (Emeryville, CA)
    …and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP ... and applicable SOPs. The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical... Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to other… more
    BeOne Medicines (12/19/25)
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  • Sr. Clinical Research Associate - Oncology - FSP

    Parexel (Sacramento, CA)
    …clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices ... Site Care Partner (SCP), and other members of the study team, as required, in activities associated with the...of sites in a clinical trial. **Monitoring Responsibilities and Study Conduct:** + Ensure proper conduct of clinical trials… more
    Parexel (12/11/25)
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  • Nurse Practitioner - Research / Physician…

    Stanford University (Stanford, CA)
    …in clinical trials. Assess physical health and administer treatments throughout the study aligned with scope of practice delegated responsibilities. Oversee study ... participant safety. . **Duties include:** + Ensure the safety of study participants, and maintain communication with their families/caregivers and clinicians. +… more
    Stanford University (11/08/25)
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  • Natural Resources Specialist

    Bureau of Reclamation (Sacramento, CA)
    …to prime agricultural lands, studies of special ecosystems, USFWS planning aid studies , study plans and others. Review and provide comments on environmental ... Fish and Wildlife Service (USFWS). Conduct environmental related public meetings with study teams and cooperating agency personnel and serve on scoping session teams… more
    Bureau of Reclamation (01/15/26)
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  • EDC/Clinical Devices Research Coordinator

    US Tech Solutions (South San Francisco, CA)
    …Clinical Research Coordinator activities for assigned clinical research device studies including consenting participants, conducting study sessions, maintaining ... and PI, is responsible for independently conducting clinical research sessions with study participants. + These sessions will be conducted on-site in South San… more
    US Tech Solutions (01/16/26)
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