A Clinical Research Coordinator (CRC) manages the daily operations of clinical trials, ensuring participant safety and protocol compliance. They recruit/screen patients, obtain informed consent, collect data, manage study documents, and report adverse events. They act as the primary liaison between investigators, sponsors, and participants.

Key Responsibilities
Coordinate day-to-day clinical trial operations at the site
Screen, recruit, and enroll study participants
Obtain and document informed consent
Schedule subject visits and follow-ups
Collect, record, and maintain accurate study data
Maintain regulatory documents and study files
Ensure compliance with study protocols and GCP guidelines
Report adverse events and safety information
Prepare for monitoring visits, audits, and inspections
Liaise with investigators, sponsors, and monitors

Required Qualifications
Bachelor’s or Master’s degree in Life Sciences / Pharmacy / Nursing / Medical field

Job Types: Full time, Permanent, Fresher

Pay: ₹18,000.00 - ₹25,000.00 per month

Perks:
Health insurance
Paid sick time

Work Location: In person

📌 Clinical Research Coordinator Only Fresher Pune
🏢 Clinova Academy
📍 Pune