Key Responsibilities
- Coordinate and manage clinical trial activities.
- Recruit and screen study participants.
- Obtain informed consent from participants.
- Schedule and conduct study visits.
- Collect and maintain accurate study data.
- Ensure compliance with study protocols and GCP guidelines.
- Report adverse events and participant safety issues.
- Maintain regulatory and study documents.
Pay: ₹16,000.00 - ₹28,000.00 per month
Benefits:
- Flexible schedule
- Paid sick time
- Provident Fund
Work Location: In person
