Clinical Research Coordinator

A Clinical Research Coordinator (CRC) manages the day-to-day operations of clinical trials. They act as the vital link between the Principal Investigator (PI), trial participants, and sponsors, ensuring trials run smoothly, safely, and in full compliance with regulatory guidelines. Key Responsibilities Patient Management: Recruit and screen potential participants, obtain informed consent, and monitor patient health throughout the study. Study Coordination: Schedule patient visits, conduct study procedures, and organize trial activities according to the protocol. Data Entry & Compliance: Accurately collect and enter clinical data, process or ship biological samples, and ensure adherence to Good Clinical Practice (GCP) standards. Administration: Maintain trial documentation and act as a liaison with study sponsors, monitors, and the Institutional Review Board #J-18808-Ljbffr