Location: Buona Vista

Working hours: Mon–Fri, 8.30am–5.30pm

Compensation: Up to $14,000/month (based on experience)

Contract role

• 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

• 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...