
Clinical Research Associate
1 week ago
Assist in setting up, monitoring, and closing clinical trial sites under supervision.
- Ensure trials are conducted in compliance with protocols, ICH-GCP guidelines, and regulatory requirements.
- Perform site visits (remote or on-site) and assist with source data verification.
- Maintain study documentation and track essential documents.
- Support the collection, review, and submission of trial-related documentation (e.g., informed consent forms, CRFs).
- Assist with training site staff on study protocols and procedures.
- Collaborate with cross-functional teams, including project managers, data managers, and regulatory staff.
- Report any deviations, issues, or safety concerns to the study lead.
- Participate in internal training programs to gain knowledge of clinical trial processes.
**Job Types**: Full-time, Fresher
Pay: ₹22,800.49 - ₹38,652.15 per month
**Benefits**:
- Health insurance
- Paid sick time
- Paid time off
Work Location: In person
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