Jobs 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.

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; review and resolve data queries; and support preparation of protocols and clinical study reports. Requires at least two years of Clinical Research Associate experience, a relevant bachelor's degree, strong knowledge of clinical trial regulations and ICH-GCP, and approximately 60% travel.

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 clinical study documentation.

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 is home-based in Australia and requires approximately 60% travel.

Supports clinical trial site monitoring and management by checking protocol, regulatory, and GCP compliance; preparing documentation; entering data; tracking site performance; maintaining accurate records; preparing monitoring reports; collaborating with cross-functional teams; and participating in training. The role requires strong organization, communication, attention to detail, and approximately 25% travel.

Negotiate and execute clinical trial site contracts and budgets, manage a portfolio of agreements, collaborate with legal/finance/project teams, maintain records, and improve templates and processes while mentoring junior staff.

Monitor clinical trial sites for protocol, regulatory, and GCP compliance; conduct site visits, resolve issues, support trial execution, and ensure data quality. Collaborate with cross-functional teams, train site staff and CRAs, manage stakeholder relationships, and oversee multiple sites and projects across domestic and international studies.

Supports clinical trial site management by coordinating site activation, tracking essential documents and approvals, maintaining trial systems, assisting CRAs with communications and queries, coordinating site visits, ensuring audit readiness, supporting site payments, and contributing to process improvements. The role requires strong organization, attention to detail, communication, collaboration, and proficiency with office and electronic systems.

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

Oversee clinical trial monitoring activities across study sites, ensuring protocol adherence, regulatory compliance, data integrity, and Good Clinical Practice standards. Conduct site visits, resolve performance issues, train site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships. The role requires independent management of multiple sites and projects, strong organizational and communication skills, and approximately 60% travel.

Serve as primary ICON liaison to investigator sites, build/maintain site relationships, support multiple studies, coordinate with clinical teams, monitor site performance and start-up timelines, gather site feedback, and drive site engagement and improvement actions.