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Senior Clinical Trials.gov Compliance Specialist
The Human Subjects Office, at the University of Iowa is seeking a Senior Clinical Trials.gov Compliance Specialist.  This position will act as education and compliance expert with regard to ClinicalTrials.gov, federal regulations, Institutional Review Board (IRB) requirements, and University of Iowa policies and procedures for the protection of human subjects involved in research. They will develop and coordinate procedures and programs to enhance investigator understanding and compliance with ClinicalTrials.gov, the HawkIRB application process, and Institutional Review Board (IRB) policies and procedures.     For additional information and a detailed job description, please visit the departmental website at:  


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