Senior Clinical Research Coordinator

Our client is seeking a Clinical Research Coordinator to lead the execution of complex clinical trials in collaboration with Principal Investigators. This role is ideal for a seasoned coordinator ready to take on independent study management, support high-profile trials, and mentor junior staff. You’ll ensure regulatory compliance, uphold research integrity, and protect participant safety while helping to advance cutting-edge treatments. Candidate will handle some managerial responsibilities. Responsibilities Oversee other CRC's while managing your own clinical trials from initiation to close-out Independently coordinate high-complexity and/or high-enrollment studies Mentor and train junior CRCs and serve as a resource on assigned projects Recruit, screen, and consent study participants in compliance with protocol Dispense investigational product and monitor adherence to study requirements Collect and process biological specimens; perform vital signs, ECGs, and phlebotomy Schedule and conduct participant visits and assessments per protocol Accurately document and enter data into EDC and resolve queries per FDA guidelines Maintain regulatory binders and ensure preparedness for monitoring visits Track and report adverse events and ensure timely SAE submissions Serve as a liaison with sponsors, monitors, and referring physicians Qualifications 3+ years as a Clinical Research Coordinator at a research site, hospital, or private practice HS Diploma or GED (Bachelors Preferred) Experience mentoring and training other research staff Experience collecting specimens (blood samples) #J-18808-Ljbffr