Job Description

Job Summary:

We are seeking a detail-oriented and organized Clinical Research Coordinator (CRC) to support and manage clinical trials in compliance with regulatory requirements and study protocols. The CRC will work closely with investigators, sponsors, and other research staff to ensure the smooth operation of clinical studies.

Key Responsibilities:

• Coordinate and manage day-to-day clinical trial activities
• Recruit, screen, and enroll study participants
• Obtain informed consent and maintain accurate documentation
• Schedule and conduct study visits and follow-ups
• Collect, process, and ship lab specimens
• Maintain study files and electronic data records (e.g., EDC systems)
• Ensure compliance with GCP, IRB, and protocol requirements
• Communicate with sponsors, monitors, and regulatory agencies as needed
• Assist with audits and monitoring visits

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