University of Cincinnati College of Medicine is seeking a Clinical Research Regulatory Specialist I to manage regulatory operations for assigned studies, coordinating submissions to IRBs and regulatory agencies. The role involves liaising with sponsors and CROs, ensuring compliance and maintaining regulatory documentation in Complion.
Primarily remote with some on-site requirements. The position requires a Bachelor's degree and 1–2 years of experience, with certifications like SOCRA/ACRP
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