Clinical Research Associate- Wound Care Experience Required

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US Accountabilities Clinical trial site monitoring: Independently conduct qualification, initiation, interim, and close-out visits, both remotely and onsite, ensuring visits are completed on schedule and documented appropriately. Monitoring reports and follow-up: Prepare accurate, timely monitoring reports detailing site issues, resolutions, actions taken, protocol deviations, study progress, and participant enrollment status. Data integrity and quality control: Review source documentation and verify case report form (CRF) data for accuracy, completeness, and consistency. Perform quality…