• Research Program Administrator - Guerin Children's…

    Cedars-Sinai (Los Angeles, CA)
    …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains research practices using Good ... responsibilities promoting activities and services associated with the Cedars-Sinai Board of Governors Innovation Center and associated Cedars-Sinai laboratories in… more
    Cedars-Sinai (06/30/25)
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  • Clinical Research Coordinator

    Actalent (Modesto, CA)
    …alongside a nurse lead. Responsibilities + Perform regulatory tasks, including IRB submissions. + Engage in sponsor correspondence, excluding budget and contracting. ... Oncology expertise + Clinical trial management + Good Clinical Practice (GCP) + IRB knowledge + Regulatory experience + Patient recruitment + Data entry proficiency… more
    Actalent (08/26/25)
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  • Project Manager, Patient Engagement…

    Norstella (Sacramento, CA)
    …the product meets customer needs and project goals. + Maintain familiarity with IRB , EC approval requirements, and GCP guidelines to ensure each project complies ... trial life cycle & processes, industry standard patient recruitment strategies, IRB /EC approval requirements, and GCP guidelines is a plus. + Detail-oriented… more
    Norstella (08/13/25)
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  • Associate Director of Clinical Theranostics…

    UCLA Fielding School of Public Health (Los Angeles, CA)
    …meet competitive conditions. Application Window Open date: July 8, 2025 Most recent review date: Monday, Aug 25, 2025 at 11:59pm (Pacific Time) Applications received ... Applications will continue to be accepted until this date, but those received after the review date will only be considered if the position has not yet been filled.… more
    UCLA Fielding School of Public Health (07/09/25)
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  • APP: NP/PA - Transitions of Care Team

    Stanford Health Care (Palo Alto, CA)
    …the supervising physician, enrolls patients in investigational studies approved by the Investigational Review Board ( IRB ), and orders the necessary tests and ... Stanford Hospital and Clinics (SHC) Medical Executive Committee and the SHC Board Credentials, Policies and Procedures Committee. This job description covers all… more
    Stanford Health Care (08/26/25)
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  • Nurse Practitioner/Physician Assistant…

    Stanford Health Care (Palo Alto, CA)
    …the supervising physician, enrolls patients in investigational studies approved by the Investigational Review Board ( IRB ), and orders the necessary tests and ... Hospital and Clinics (SHC) Medical Executive Committee and the SHC Board Credentials, Policies and Procedures Committee. **Locations** Stanford Health Care **What… more
    Stanford Health Care (08/26/25)
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  • Research Nurse Coordinator I, Oncology (Hybrid)

    Cedars-Sinai (Beverly Hills, CA)
    …and/or procedures as required and ensures protocol is followed. + May prepare IRB submissions. + May process, ship, track or otherwise handle research specimens. + ... May perform data entry **Qualifications** **This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area.**… more
    Cedars-Sinai (08/21/25)
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  • Research Assistant - Urology

    UCLA Health (Los Angeles, CA)
    …the mission and goals of assigned program/project, may include works related to IRB protocol submission and approval. Supports the effort to ensure compliance with ... all UCLA as well as relevant federal and state regulations. + Collaborating in working toward the completion of all program/project activities, research, outreach, and recruitment. Work with research participants on consent and surveys/interviews. Assists with… more
    UCLA Health (08/20/25)
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  • Senior Biostatistician

    J&J Family of Companies (Irvine, CA)
    …all phases of clinical studies of moderate complexity under limited supervision. + Review clinical study protocols and Case Report Forms (CRFs) for proposed studies ... unblind treatment assignments and handle unblinded information appropriately. + Support the review and assessment of protocol deviations to the extent that they… more
    J&J Family of Companies (08/20/25)
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  • RayzeBio Director, Medical Affairs Research…

    Bristol Myers Squibb (San Diego, CA)
    …market value assessments for all study related items. Create process for internal review of budgeting of trials + Maintain all internal records and databases ... ensure that all investigator-initiated trials adhere to relevant regulatory guidelines, including IRB approvals and IND submissions + Maintain safety data from all… more
    Bristol Myers Squibb (08/19/25)
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