Clinical Research Monitor

About the role

This fully remote Clinical Research Monitor role focuses on supporting IND‑regulated clinical trials within an academic research environment. The position centers on risk-based monitoring, Trial Master File (TMF) management, and ensuring adherence to FDA regulations, IND/IDE requirements, and Good Clinical Practice (GCP) guidelines. You will work autonomously while collaborating closely with research, regulatory, and compliance leaders to support high-profile breast imaging and interventional breast procedure studies. This newly created role offers significant visibility, strong potential for extension beyond the initial contract term, and the opportunity to gain valuable experience