Description Clinical/Translational Research Coordinator II Knowledge and understanding of policies, procedures, and regulations governing human subject's research Knowledge and understanding of the Federal regulations and guidelines governing the protection of human subjects, e.g., FDA, OHRP, GCP/ICH, and HIPAA regulations. Proficiently prepares and processes new IRB research proposals, amendments, continuing review applications and adverse event reports according to institutional and departmental policies and procedures and federal regulations. Procures equipment for clinical research Manages Protocols and participates in recruitment/enrollment of study participants Understands and Impleme
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