Participate in the design, execution, and management of clinical and translational research studies in urologic oncology Assist with study development, including protocol writing, IRB submissions, regulatory documentation, and data management plans Conduct data collection, curation, quality
Research Project and Regulatory Management: Assist Principal Investigator(s) with implementation and coordination of clinical, translational, and health services research projects within the Department of Urology. Prepare, submit, and maintain regulatory documentation including IRB applications, protocol amendments,