Teams at ICON plc

Manage day-to-day clinical trial operations, including planning, timelines, budgets, protocols, stakeholder relationships, regulatory compliance, vendor selection, risk management, and clinical deliverables. Support cross-functional teams and develop team members while ensuring high-quality study outcomes. The role requires a relevant university degree, therapeutic-area expertise, clinical trial management experience, and approximately 25% travel.

Supports the coordination and administration of clinical trials, including maintaining study files, preparing trial materials, managing regulatory documentation, coordinating cross-functional communication, and tracking clinical trial milestones and metrics while ensuring protocol and regulatory compliance.

Supports the coordination and administration of clinical trials, including maintaining study files, preparing regulatory and study materials, facilitating cross-functional communication, and tracking trial metrics and milestones. Ensures compliance with protocols, regulations, and guidelines while contributing to high-quality clinical research delivery.