- Assist in the monitoring and management of clinical trials under the guidance of senior CRAs.
- Support site selection, initiation, monitoring, and close-out activities.
- Review clinical trial documents for completeness, accuracy, and compliance.
- Assist with maintaining the Trial Master File (TMF) and Investigator Site Files (ISF).
- Support collection and review of essential regulatory and study documents.
- Communicate with clinical sites, investigators, study coordinators, and internal project teams.
- Identify and report protocol deviations, data discrepancies, and site-related issues.
- Assist with ensuring compliance with ICH-GCP, SOPs, protocols, and applicable regulatory requirements.
- Prepare and maintain monitoring reports and study-related documentation.
- Participate in study meetings, training sessions, and other clinical research activities.

Pay: ₹22,000.96 - ₹35,000.00 per month

Perks:

- Cell phone reimbursement
- Commuter assistance
- Flexible schedule
- Food provided
- Paid sick time
- Paid time off
- Provident Fund

Work Location: In person

📌 Clinical Research Associate (India)
🏢 Cliniweb Services
📍 India