Clinical Research Coordinator
CurrentInterpreted and implemented complex protocol requirements to minimize deviations and ensure compliance.Identified and recommended candidates to physicians for up to 20 clinical trials at a time to increase enrollment.Documented study procedures thoroughly and meticulously for streamlined data collection and reporting in a variety of Electronic Data Capture systems.Scheduled and organized appointments and scans across institutions to reduce friction and complete study tasks in a timely manner.Complied with principles of GCP and IRB, FDA and HIPPA requirements. Entered and monitored data in multiple EDC, IVRS and ePRO systems to ensure correct data capture.