Clinical Research Associate
2 days ago
- Assist in setting up, monitoring, and closing clinical trial sites as per study protocols.
- Support investigators and site staff in maintaining accurate study documentation.
- Perform remote and onsite monitoring visits under supervision.
- Ensure proper collection, verification, and reporting of clinical trial data.
- Assist in reviewing Case Report Forms (CRFs) for accuracy and completeness.
- Ensure compliance with Good Clinical Practice (GCP), SOPs, and regulatory guidelines.
- Help with trial supplies tracking, site communication, and documentation management.
- Prepare monitoring visit reports and follow-up letters with oversight.
- Coordinate with cross-functional teams including data management, safety, and regulatory affairs.
Job Types: Full-time, Permanent, Fresher
Pay: ₹24, ₹45,599.86 per month
Benefits:
- Cell phone reimbursement
- Health insurance
- Paid sick time
- Paid time off
- Provident Fund
- Work from home
Work Location: In person
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