Position Overview
Location: Buona Vista
Working hours: Mon–Fri, 8.30am–5.30pm
Compensation: Up to $14,000/month (based on experience)
Contract role
Key Responsibilities - Lead operational planning and execution of clinical studies
- Coordinate between CRU and sponsor cross-functional teams
- Ensure adherence to study protocols, timelines, and regulatory requirements
- Support IRB/regulatory submissions and operational alignment
- Drive communication, issue resolution, and study performance tracking
- Maintain study documentation, metrics, and operational databases
- Lead post-study reviews and process improvements
- Supervise and guide CRU team members
Requirements - Degree in Science / Health / Life Sciences or related field
- Minimum 5 years clinical research experience (PM/operations)
- Experience in early-phase clinical trials preferred
- Strong l...