Key Responsibilities:
- Coordinate and manage clinical research studies.
- Recruit, screen, and enroll eligible participants.
- Obtain informed consent from study participants.
- Schedule participant visits and maintain study records.
- Collect, document, and manage clinical trial data accurately.
- Ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
- Report adverse events and maintain participant safety.
- Communicate with investigators, sponsors, and ethics committees.
- Prepare for monitoring visits, audits, and inspections.
- Maintain essential study documents and regulatory files.
Pay: ₹15,000.00 - ₹25,000.00 per month
Benefits:
- Paid sick time
- Provident Fund
Work Location: In person
