Jobs at ICON plc

Support site activation, document collection and maintenance, CTMS updates, site communications, visit logistics, and document filing to ensure compliant, audit-ready clinical trial operations while assisting CRAs and project teams.

Serve as primary ICON liaison to investigator sites, build strong long-term relationships, support multiple studies, align site capabilities with study needs, monitor site performance and metrics, drive improvements, and contribute to site engagement strategies and process enhancements.

The Study Start-Up Specialist will manage study initiation, drive regulatory compliance, support project teams, and ensure patient safety in clinical trials in Australia.

As a Clinical Research Associate, you'll conduct site visits for clinical trials, ensuring compliance and data integrity, and collaborating with investigators.

As a CRA II, you will design and analyze clinical trials, conduct site visits, ensure protocol compliance, and collaborate with investigators while maintaining data integrity and patient safety.

As a CRA II, you'll conduct and monitor clinical trials, ensure compliance and data integrity, and collaborate with site staff and investigators.