
Clinical Research Coordinator
3 weeks ago
- Assist in the coordination and conduct of clinical trials under supervision
- Support patient recruitment, screening, and enrollment according to protocol criteria
- Schedule and manage patient visits, sample collection, and follow-ups
- Collect and accurately enter data into Case Report Forms (CRFs) or Electronic Data Capture (EDC) systems
- Maintain essential documents in the Investigator Site File (ISF)
- Ensure adherence to study protocols, ICH-GCP, and regulatory requirements
- Assist in the preparation for audits or monitoring visits
- Communicate with sponsors, CROs, and ethics committees as needed
- Ensure timely reporting of adverse events and protocol deviations
- Support inventory management of study drugs, lab kits, and trial materials
Job Types: Full-time, Permanent, Fresher
Pay: ₹19, ₹34,468.52 per month
Benefits:
- Health insurance
- Paid sick time
Work Location: In person
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