Clinical Research Coordinator

Clinical Research Coordinator

1. Coordinate clinical trials, including study start-up, daily activities and close-out.

2. Ensure compliance with study protocols, GCP guidelines and regulatory requirements.

3. Support patient screening, informed consent, study assessments and timely adverse event reporting.

4. Maintain accurate study data, trial documents and specimen records, and support monitoring visits and audits.

5. Track trial expenses and support timely invoicing and research account closure

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