The Regulatory Coordinator is responsible for overseeing the day-to-day regulatory management of all types of clinical research protocols. The position will manage all aspects of study start-up, modification submissions, continuous reporting, and study close-out to the Institutional Review Board (IRB) and any relevant regulatory agencies including, the Institutional Biosafety Committee, the institutional Radiation Safety Committee, and the clinical trial sponsor, funding foundation, or governmental agency. Manage day-to-day regulatory operations and workload of regulatory team, plan resource needs and strategize growth. Provide regulatory support for research programs and oversee maintenance of all required regulatory documents.