01Overview
Monitor clinical trial sites to ensure compliance with study protocols, GCP, and regulatory requirements.
- Perform site initiation, routine monitoring, and close-out visits.
- Review and verify case report forms (CRFs) against source documents.
- Identify and resolve data discrepancies.
- Ensure proper documentation and timely reporting of adverse events.
- Maintain effective communication with investigators, sponsors, and regulatory authorities.
- Assist in the preparation of regulatory submissions and documentation.
- Provide training and support to site staff as needed.
- Participate in study team meetings and contribute to study planning and protocol development.
Job Types: Permanent, Fresher
Compensation: 24,000.03 - 37,729.97 per month
Perks:
- Health insurance
- Provident Fund
Schedule:
- Day shift
Supplemental Compensation:
- Performance bonus
Work Location: In person .
