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Cincinnati Children's Hospital Medical Center Logo
Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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Akron Children's Hospital

Akron, Ohio

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Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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Vanderbilt Health

Nashville, Tennessee

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Cincinnati Children's Hospital Medical Center Logo
Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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Cincinnati Children's Hospital Medical Center Logo
Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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Vanderbilt Health

Nashville, Tennessee

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Cincinnati Children's Hospital Medical Center Logo
Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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Nicklaus Children’s Health System

Miami, Florida

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Vanderbilt Health

Nashville, Tennessee

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Vanderbilt Health

Nashville, Tennessee

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Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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BJC HealthCare

Saint Louis, Missouri

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BJC HealthCare

Saint Louis, Missouri

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Cincinnati Children's Hospital Medical Center Logo
Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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Cincinnati Children's Hospital Medical Center Logo
Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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Nicklaus Children’s Health System

Miami, Florida

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Vanderbilt Health

Nashville, Tennessee

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Vanderbilt Health

Nashville, Tennessee

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Vanderbilt Health

Nashville, Tennessee

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Western Michigan University Homer Stryker M.D. School of Medicine

Kalamazoo, Michigan

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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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