Teams at ICON plc

Conduct clinical trial site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; resolve data queries; and support preparation and review of protocols and clinical study reports. The role requires approximately 60% travel.

Oversee clinical trial monitoring activities, ensuring site adherence to protocols, regulations, and GCP standards. Conduct site visits, resolve performance issues, support data integrity, train site personnel and CRAs, and collaborate with cross-functional stakeholders. Manage multiple sites and projects independently while maintaining strong relationships and driving compliance. The role is home-based in Australia and requires approximately 60% travel.

Independently negotiates and executes clinical trial site contracts and budgets for multiple studies. Reviews contract language, manages negotiation portfolios and timelines, resolves issues with legal, finance, and project teams, maintains accurate contract records, improves templates and processes, and mentors junior colleagues. Requires relevant contracts experience in CRO, pharmaceutical, or healthcare settings, knowledge of clinical trial agreements, and strong negotiation and organizational skills.