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
Versatile schedule
Food provided
Paid sick time
Paid time off
Provident Fund

Work Location: In person

📌 Clinical Research Associate Mumbai
🏢 Cliniweb Services
📍 Mumbai