Clinical Research Associate- Wound Care

From the original posting

Canada Accountabilities Clinical trial site monitoring: Conduct site qualification, initiation, interim, and close-out visits remotely and onsite, ensuring appropriate documentation, timely follow-up, and adherence to study protocols. Monitoring reports and documentation: Prepare accurate and timely monitoring visit reports covering site issues, resolutions, corrective actions, protocol deviations, study progress, and enrollment status. Data integrity and quality assurance: Review source documents and verify case report form (CRF) data to ensure accuracy, completeness, and consistency.…