• Clinical Research Associate I - Miriad IBD Biobank…

    Cedars-Sinai (Los Angeles, CA)
    …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, ... local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains research practices using Good Clinical… more
    Cedars-Sinai (08/27/25)
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  • Clinical Research Data Specialist I - Heart…

    Cedars-Sinai (Los Angeles, CA)
    …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . ESSENTIAL JOB DUTIES AND RESPONSIBILITIES: Manages ... agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . Maintains research practices using Good Clinical Practice… more
    Cedars-Sinai (08/24/25)
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  • Bilingual Clinical Research Associate I - Ramin…

    Cedars-Sinai (Los Angeles, CA)
    …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, ... local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains research practices using Good Clinical… more
    Cedars-Sinai (08/01/25)
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  • Clinical Research Associate I- Smidt Heart…

    Cedars-Sinai (Los Angeles, CA)
    …for long term follow-up patients only. *Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, ... agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . *Maintains research practices using Good Clinical Practice… more
    Cedars-Sinai (07/16/25)
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  • Heart Institute Clinical Research Assoc I/CPT…

    Cedars-Sinai (Los Angeles, CA)
    …follow-up patients only. + Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse ... agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . Maintains research practices using Good Clinical Practice… more
    Cedars-Sinai (07/02/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …for completion and accuracy with source documents. Prepare regulatory submissions and ensure Institutional Review Board renewals are completed. + Monitor ... REDCap and database applications + Demonstrated knowledge of regulatory requirements including Institutional Review Boards, HIPAA and Good Clinical Practices +… more
    Stanford University (08/07/25)
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  • Cancer Clinical Research Coordinator Associate…

    Stanford University (Stanford, CA)
    …for completion and accuracy with source documents. Prepare regulatory submissions, and ensure Institutional Review Board renewals are completed. + Assemble ... and recording of patient and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor visits and regulatory audits.… more
    Stanford University (08/30/25)
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  • Cancer Clinical Research Coordinator Associate…

    Stanford University (Stanford, CA)
    …for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board renewals are completed. + Assemble ... and recording of patient and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor visits and regulatory audits.… more
    Stanford University (08/30/25)
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  • Clinical Research Coordinator Associate…

    Stanford University (Stanford, CA)
    …for completion and accuracy with source documents.Prepare regulatory submissions, and ensure institutional Review Board renewals are completed. + Assemble ... and recording of patient and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor visits and regulatory audits.… more
    Stanford University (08/19/25)
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  • Clinical Research Coordinator Associate (1 Year…

    Stanford University (Stanford, CA)
    …for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board renewals are completed. + Assemble ... and recording of patient and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor visits and regulatory audits.… more
    Stanford University (08/07/25)
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