Clinical Research Associate
5 days ago
Monitor clinical trial sites to ensure compliance with study protocols, GCP, and regulatory requirements.
- Perform site initiation, routine monitoring, and close-out visits.
- Assist in the preparation of regulatory submissions and documentation.
- Provide training and support to site staff as needed.
- Review and verify case report forms (CRFs) against source documents.
- Identify and resolve data discrepancies.
- Ensure proper documentation and timely reporting of adverse events.
**Job Types**: Permanent, Fresher
Pay: ₹25,001.03 - ₹40,100.97 per month
**Benefits**:
- Health insurance
- Provident Fund
Schedule:
- Day shift
Supplemental Pay:
- Performance bonus
Work Location: In person
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