Working collaboratively with principal investigators, physicians, clinical research coordinators, university offices, sponsors, and external research partners, the Clinical Research Regulatory Manager facilitates efficient regulatory workflows, supports timely study activation and ongoing compliance, and promotes consistent regulatory practices across clinical research activities. Clinical Trial Monitoring and Coordination: Participate in clinical trial monitoring activities as appropriate and collaborate with investigators, physicians, study coordinators, and research partners to address regulatory documentation needs and support adherence to approved protocols and applicable requirements.