Study Delivery Associate

About the role

The Study Delivery Associate provides essential administrative and operational support to clinical trial management activities. This role supports the Study Delivery T eam in meeting study timelines, ensuring regulatory compliance, and executing standardized processes related to clinical trial coordination, document and system management.

What you'll do

• Support the setup and maintenance of study-level trackers, dashboards and timelines
• Communicate study progress, timelines and deliverables to the Study Delivery Manager
• Assist with tracking and following up on study actions, including risk mitigation actions
• Assist with the preparation and record keeping of risk & quality reviews
• Ensure completion of study team training and inspection readiness activities to maintain compliance with regulatory requirements

What you need

• 6–11 yrs of experience
• Regulatory affairs
• PowerPoint
• Clinical research
• Reconciliation
• CRO
• Diploma