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Clinical Research Associate
2 weeks ago
Assist in setting up, monitoring, and closing clinical trial sites under supervision.
- Ensure trials are conducted in accordance with ICH-GCP guidelines, regulatory requirements, and company SOPs.
- Review case report forms (CRFs) for completeness, accuracy, and consistency.
- Assist with study documentation including investigator site files (ISFs), trial master files (TMFs), and essential documents.
- Collaborate with investigators, site staff, and internal teams to support smooth trial execution.
- Track and manage study supplies and ensure compliance with study protocols.
- Participate in investigator meetings, site initiation visits, and training sessions.
**Job Types**: Full-time, Permanent, Fresher
Pay: ₹22,821.77 - ₹35,967.25 per month
**Benefits**:
- Health insurance
- Provident Fund
Schedule:
- Day shift
Supplemental Pay:
- Performance bonus
- Yearly bonus
Work Location: In person