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Regina Oegerle has gained extensive experience in the clinical research industry, working in various roles such as an Account Associate at Univo IRB, a Study Start Up Lead at IQVIA Biotech, a Start Up Specialist at Covance, a Regulatory Specialist, and a Scheduling Coordinator at Florida Urology Center. In their current role, Regina specializes in the ethical review of pharmaceutical, device, biologic, behavioral, and psycho-social research studies. Through their career, Regina has developed skills in preparing clinical research protocols, informed consent forms, applications, and coordinating various aspects of clinical trials.