Clinical Research Coordinator
Medix
Participant Management: Recruit, screen, and enroll eligible study participants. Obtain informed consent and monitor participant safety and compliance throughout the trial. Study Coordination: Coordinate daily study visits, procedures, and follow-ups according to the study protocol. Data Management: Collect, record, and manage accurate source documentation and enter data into Electronic Data Capture (EDC) systems. Address data queries promptly. Regulatory & Compliance: Ensure adherence to Good Clinical Practice (GCP) guidelines, federal regulations, and Institutional Review Board (IRB) requirements. Assist with regulatory documents and safety reporting. Communication & Liaison: Serve as the main point of contact for patients, investigators, monitors, and study sponsors #J-18808-Ljbffr
Vacancy posted 3 days ago
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