• Clinical Research Coordinator I - Torres Lab…

    Cedars-Sinai (Los Angeles, CA)
    …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **Primary Duties and Responsibilities** + ... ensure smooth coordination. + Assist with regulatory submissions to the Institutional Review Board (IRB), including Adverse Events, Serious Adverse Events,… more
    Cedars-Sinai (08/29/25)
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  • Clinical Research Coordinator III - Miriad IBD…

    Cedars-Sinai (Los Angeles, CA)
    …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **Primary Job Duties and Responsibilities:** ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
    Cedars-Sinai (08/27/25)
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  • Senior Research Coordinator in Precision…

    Stanford University (Stanford, CA)
    …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions and respond to ... New Drug applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are completed. + Managing the execution of… more
    Stanford University (08/23/25)
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  • Clinical Research Coordinator III - Guerin…

    Cedars-Sinai (Los Angeles, CA)
    …all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **What are the Primary Duties & ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
    Cedars-Sinai (08/01/25)
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  • Clinical Research Coordinator II, Thoracic…

    Cedars-Sinai (CA)
    …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and Responsibilities + ... conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
    Cedars-Sinai (07/29/25)
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  • Clinical Research Coordinator II / CPT - Emergency…

    Cedars-Sinai (Beverly Hills, CA)
    …all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **What are the Primary Duties and ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
    Cedars-Sinai (07/18/25)
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  • Clinical Research Coordinator I, Per Diem - Thai…

    Cedars-Sinai (Los Angeles, CA)
    …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and Responsibilities + ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
    Cedars-Sinai (06/05/25)
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  • Cancer Clinical Research Coordinator 2 - Radiation…

    Stanford University (Stanford, CA)
    …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... New Drug applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are completed. _* - Other duties may… more
    Stanford University (08/08/25)
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  • Clinical Research Coordinator I - Department…

    Cedars-Sinai (Los Angeles, CA)
    …and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board . **_*This position is hybrid*_** **Primary Duties ... + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events,… more
    Cedars-Sinai (07/23/25)
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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 ... New Drug applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are completed. + Hybrid work agreement. _*… more
    Stanford University (08/21/25)
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