
Clinical Research Associate
2 days ago
- Assist in monitoring clinical trials at investigational sites under supervision
- Ensure compliance with ICH-GCP guidelines, regulatory requirements, and company SOPs
- Support site initiation, routine monitoring, and close-out visits
- Help in verifying source data and case report forms (CRFs)
- Maintain study documentation and track trial progress
- Assist in identifying and resolving site issues and deviations
- Coordinate with investigators, site staff, and internal study team
- Participate in training programs and development activities
- Prepare visit reports and documentation under supervision
- Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field
Job Types: Full-time, Permanent, Fresher
Pay: ₹23, ₹38,990.58 per month
Benefits:
- Health insurance
- Paid sick time
- Provident Fund
Work Location: In person
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