Job Description

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: ₹19,715.80 - ₹34,468.52 per month

Benefits:

Health insurance Paid sick time
Work Location: In person