Project Coordinator, eCOA

📋 Description

• Support Project Managers throughout the planning, setup, monitoring, and closeout phases of eCOA
• Coordinate study database setup, project documentation, operational activities, and key
• Maintain accurate and organized project records and study documentation throughout the project
• Coordinate the distribution, tracking, reconciliation, and logistics of study devices and equipment.
• Prepare and distribute project reports, status updates, meeting materials, and study communications.
• Organize Project Assurance meetings, record minutes, and monitor action items through completion.

🎯 Requirements

• Bachelor’s degree preferred, or an equivalent combination of education and relevant professional
• 1–3 years of experience in pharmaceutical, biotechnology, clinical research, healthcare, life
• Understanding of the drug development process and clinical trial environment.
• Previous experience supporting eCOA, ePRO, eConsent, clinical technology, or other
• Strong organizational, planning, prioritization, and time-management skills.
• Excellent attention to detail and commitment to accurate, high-quality work.

🎁 Benefits

• Competitive pay and incentive opportunities.
• Provident fund contributions.
• Medical insurance.
• Engaging employee programs and local events.
• Access to modern office facilities.