- 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 (Mumbai)
🏢 Cliniweb Services
📍 Mumbai