INSTITUTIONAL REVIEW BOARD (IRB) COMPLIANCE ADMINISTRATOR, Office of the Vice President for Research, to conduct ethical and compliance reviews to ensure compliance with applicable laws and regulations for the use of human subjects in research.  Will serve as a point of contact (POC) and compliance reviewer of human subject research protocols; conduct research protocol reviews to identify regulatory and other issues and identify potential risks to research participants; correspond with and advise investigators, articulating modifications to study documentation; write high-level protocol summaries, coordinate ancillary reviews, and advise colleagues/investigators on navigating the regulatory landscape and applicability of regulations; manage and evaluate single IRB reliance requests and serve as POC for SMART IRB; direct communications between relying and reviewing institutions and carry out reliance actions; serve as a clinicaltrials.gov registration representative; assist with developing educational materials and conduct workshops/presentations; assist with COUHES Connect; maintain knowledge of federal/state/local regulations; and support other functions as needed.