• 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 ... complete study documents/case report forms. + Ensure compliance with research protocols, and review and audit case...+ Ensure essential documentation and recording of patient and research data in appropriate files per institutional more
    Stanford University (08/07/25)
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  • Clinical Research Associate I - Butte Lab…

    Cedars-Sinai (Los Angeles, CA)
    …contact for long-term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of ... **Dr. Pramod Butte, Ph.D. is looking for a Clinical Research Associate I to join a diverse team!** The...billing. This role will follow all federal, local, FDA, IRB , and HIPAA guidelines and regulations pertaining to the… more
    Cedars-Sinai (08/23/25)
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  • Clinical Research Coordinator I (Part-Time)…

    Cedars-Sinai (Santa Monica, CA)
    … staff meetings. + Works closely with investigators and regulatory staff or directly with Institutional Review Board ( IRB ) to submit adverse events, ... **Are you ready to be a part of breakthrough research ?** The Clinical Research Coordinator I supports...requirements, including but not limited to Sponsor, FDA, and IRB requirements. + Ability to use software applications (MS… more
    Cedars-Sinai (08/14/25)
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  • Social Science Research Professional 1,…

    Stanford University (Stanford, CA)
    …strategies for recruitment, data quality control procedures and processes). May follow up with Institutional Review Board ( IRB ) to ensure renewals are ... presentations. + Co-authorship on published papers experience with creating and managing IRB documentation. + Maintaining research team adherence to regulatory… more
    Stanford University (08/07/25)
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  • Cancer Clinical Research Coordinator 2 - GI…

    Stanford University (Stanford, CA)
    …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Cancer Clinical Research Coordinator 2 - GI (Hybrid) **School of...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… more
    Stanford University (08/21/25)
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  • Clinical Research Coordinator 2

    Stanford University (Stanford, CA)
    …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Clinical Research Coordinator 2 **School of Medicine, Redwood City,...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… more
    Stanford University (08/19/25)
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  • Cancer Clinical Research Coordinator 2…

    Stanford University (Stanford, CA)
    …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Cancer Clinical Research Coordinator 2 - Radiation Oncology CCSB (Hybrid)...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… more
    Stanford University (08/08/25)
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  • Clinical Research Coordinator II

    Stanford University (Stanford, CA)
    …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Clinical Research Coordinator II **School of Medicine, Stanford, California,...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… more
    Stanford University (08/07/25)
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  • Cancer Clinical Research Coordinator…

    Stanford University (Stanford, CA)
    …for completion and accuracy with source documents. Prepare regulatory submissions, and ensure Institutional Review Board renewals are completed. + Assemble ... complete study documents/case report forms. + Ensure compliance with research protocols, and review and audit case...+ Ensure essential documentation and recording of patient and research data in appropriate files per institutional more
    Stanford University (08/21/25)
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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 ... completing study documents and forms. + Ensure compliance with research protocols, review and audit study forms...and/or preprocessing fMRI data + Knowledge of human subjects research regulations ( IRB , informed consent, HIPAA) +… more
    Stanford University (08/20/25)
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