The Clinical Research Coordinator (CRC) is an experienced research professional who works collaboratively with clinical research site management and the Principal Investigator (PI) to support the successful execution of clinical trials. While the PI maintains overall responsibility for the conduct of the study, the CRC independently manages and coordinates day-to-day clinical trial activities, ensuring protocol compliance, data integrity, and operational efficiency. The CRC also serves as a resource and mentor to research staff and contributes to study oversight, workflow optimization, and team development. Essential Duties and Responsibilities: Assist the Investigator in screening and reviewing potential study participant eligibility in accordance with protocol requirements Maintain accurate and timely case report forms, source documentation, study charts, and regulatory documentation Provide mentorship, training, and day-to-day oversight to Clinical Research Coordinators and Research Assistants Ensure all clinical research activities are conducted in compliance with study protocols, GCP guidelines, sponsor requirements, and applicable laws, regulations, policies, and procedures Collect, review, and enter study data with a high degree of accuracy and attention to detail Support management in the candidate interview, selection, onboarding, and shadowing processes for new hires Assist with study start-up activities, ongoing study maintenance, and close-out procedures across assigned studies and team initiatives Collaborate with investigators, sponsors, CROs, and internal departments to facilitate efficient study operations and issue resolution Demonstrate the ability to independently prioritize workload and adapt to changing study needs and assignments Serve as a resource for team members regarding study processes, protocol requirements, and site procedures