A seasoned clinical research professional, Cy Gill oversees Univo IRB’s compliance with human research protection regulations and guidelines. Cy represents Univo IRB in regulatory inspections, AAHRPP site visits, and customer audits. He has held essential clinical operations leadership positions with sponsors and contract research organizations (CROs) in the biotech, pharmaceutical, and medical device space. Over his career, he served on two central IRBs and has monitored and overseen countless clinical trials in all phases and major therapeutic areas. Cy also has hands-on clinical experience, making him uniquely equipped with the understanding to provide relevant safeguards for the protection of human research. He holds a Bachelor of Science in nursing, Master of Science in clinical research management, and is a Master of Business Administration candidate.
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