Clinical Trial Coordinator - (FSP )

About the role

As part of our global team, you’ll have the opportunity to provide administrative and technical support to the Project Team. As a Clinical Trial Coord, you'll support audit readiness by ensuring files are reviewed according to the schedule detailed in the organization's SOP and department guidance document.

What you'll do

• Provide support for critical day-to-day clinical study activities, including regulatory inspection readiness
• Collaborate with Clinical Operations/Study Manager, study teams, and Clinical Research Organizations (CROs) to support clinical study activities as defined by the…
• Review of study documentation, including essential document packets, study plans, informed consent forms, etc
• Supporting/oversight of risk-based monitoring
• Attendance of key team meetings as required, including Minutes for selected studies

What you need

• 2–5 yrs of experience
• SOP writing
• PowerPoint
• Clinical research
• Documentation
• Reconciliation
• Communication
• Any graduate