Clinical Research Coordinator

Responsibilities: Review and understand each study protocol before start up, working closely with the PI and Site Director. Screen, consent, and enroll study volunteers, then schedule and manage their visits. Maintain accurate and complete study records, including source documents, regulatory files, and CRFs. Track and report adverse events and protocol deviations in line with GCP and FDA requirements. Communicate protocol related questions and updates to the sponsor and site leadership. Support subject recruitment efforts and maintain ongoing communication with referring providers.

Requirements: High school diploma required, college degree preferred. Two to four years of clinical research coordination experience or CRC certification. Phase I clinical trial experience required. Strong knowledge of GCP, ICH guidelines, and medical terminology. Excellent verbal and written communication skills. Proficiency in Word, Excel, and clinical trial management systems.