Senior ClinicalTrials.gov Compliance Specialist

The Human Subjects Office (HSO) is seeking a Senior Compliance Specialist, to specialize with ClinicalTrials.gov, to develop and coordinate programs that will enhance investigator understanding and compliance with ClinicalTrials.gov, the HawkIRB application process, and Institutional Review Board (IRB) policies and procedures.  The Senior ClinicalTrials.gov Compliance Specialist will act as the education and compliance expert with regard to ClinicalTrials.gov, federal regulations, IRB requirements, and University of Iowa policies and procedures for the protection of human subjects involved in research.  Occasional in-state and out-of-state travel is required to attend conferences and meetings.

For more information, please see: https://research.uiowa.edu/office-vice-president-research/open-positions

To apply:  See requisition 19005046 at https://jobs.uiowa.edu

Applicable background checks will be conducted.

The University of Iowa is an equal opportunity/affirmative action employer. All qualified applicants are encouraged to apply and will receive consideration for employment free from discrimination on the basis of race, creed, color, national origin, age, sex, pregnancy, sexual orientation, gender identity, genetic information, religion, associational preference, status as a qualified individual with a disability, or status as a protected veteran.