Clinical Research Coordinator 258108

Medix™; Beverly Hills (CA); On-site; USD 65,000 - 90,000; Full time

Job summary

Medix™ is seeking a Clinical Research Coordinator in Beverly Hills, CA to support participant management, study coordination, data capture, and regulatory compliance across trials.

You will recruit and screen participants, coordinate visits, manage EDC data, ensure GCP adherence, and serve as the primary liaison among patients, investigators, monitors, and sponsors. This on-site role demands meticulous documentation and timely safety reporting.

Responsibilities

• Recruit, screen, and enroll eligible study participants; obtain informed consent and monitor safety and compliance.
• Coordinate daily study visits, procedures, and follow-ups per the study protocol.
• Collect, record, and manage source documentation; enter data into EDC systems; address data queries promptly.
• Ensure adherence to GCP, federal regulations, and IRB requirements; assist with regulatory documents and safety reporting.
• Serve as the main point of contact for patients, investigators, monitors, and study sponsors.

Job description

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