• Regulatory Specialist - CRI

    Methodist Health System (Dallas, TX)
    …team members for clinical trials assigned. * Assist in the development of clinical trial documents for signature of principal investigator and approval by the IRB. * ... Create and/or adapt clinical trial informed consent documents for Institutional Review Board (IRB)...(ICH) and Good Clinical Practice (GCP) guidelines. * Attend study specific training, investigator meetings as assigned, and MHS… more
    Methodist Health System (01/17/24)
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