CLINICAL RESEARCH COORDINATOR Dr. Richard H. Weisler, MD, PA and Associates
Raleigh, NC
05.2018 - 02.2024
Analyzed workflows to ensure regulatory compliance Prepared analytical reports and formal correspondence Managed high-volume correspondence and responded to complex inquiries Managed IRB submissions and regulatory documentation Coordinated industry-sponsored clinical trials Screened subjects and conducted informed consent Maintained EDC data accuracy and resolved issues Supported staff with protocol and compliance training Led operational and regulatory activities for clinical trials Submitted IRB applications, renewals, and amendments Oversaw participant recruitment, screening, and consent processes Monitored study timelines and boosted enrollment by 75% Maintained data integrity through EDC oversight and remediation planning Conducted internal monitoring and regulatory document review Supported study start-up, maintenance, and closeout activities Ensured compliance with protocols and guidelines Supported subject screening and consent processes Ensured adherence to protocol and regulatory standards Maintained compliance documentation and records Show Description