Jobs at ICON plc

The Clinical Research Associate will oversee site compliance, conduct visits, monitor patient safety, and collaborate with cross-functional teams in clinical studies.

Serve as primary contact between investigational sites and sponsor to conduct site selection, initiation, routine monitoring, and close-out. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor patient safety (AE/SAE/PQC), support recruitment and drug accountability, resolve data queries, track site training and budgets, escalate risks, and collaborate with cross-functional clinical teams.

Lead on-site clinical monitoring for oncology/hematology trials: conduct site selection, initiation, routine and close-out visits; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor patient safety and AE/SAE reporting; oversee drug accountability, support recruitment and retention, resolve data queries, track site budgets, and escalate risks to clinical teams while collaborating cross-functionally.

Oversee the implementation of IRT solutions for clinical trials, managing project planning, execution, and stakeholder communication.

As a Clinical Research Associate, you will oversee clinical trial activities, ensuring compliance with protocols and regulations, and provide support to trials.

Lead regional clinical operations projects: develop and execute project plans, manage cross-functional teams, mentor staff, define scope with stakeholders, produce project documentation and reports, integrate industry best practices, and support organizational growth. Travel approximately 25%.

The Senior CRA will oversee clinical trial activities, ensuring adherence to protocols and regulatory requirements while managing multiple sites and projects.

The Senior Clinical Research Associate will conduct site visits, ensure trial compliance, review data, and prepare study documentation.

Perform site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; review data and queries; collaborate with site staff; and help prepare study documentation and reports.

The Clinical Research Associate will manage clinical trials, ensure compliance and data integrity, and collaborate with site staff and investigators.

The Clinical Research Associate will manage clinical trial processes including site visits, data integrity, and prepare study documentation to ensure compliance and patient safety.

As a Clinical Research Associate, conduct site visits, ensure compliance and safety, collaborate with staff, and review clinical data documentation.

The Senior Clinical Research Associate will manage clinical trials, ensure compliance, analyze data, and collaborate with study personnel while traveling extensively.

The Clinical Research Associate will conduct site visits for clinical trials, ensuring compliance and data integrity, and collaborating with site staff and investigators.

Conduct site qualification, monitoring, and close-out visits for clinical trials while ensuring compliance and data integrity. Collaborate with investigators and prepare study documentation.

The Feasibility Principal Analyst leads feasibility activities for clinical studies, analyzes data for enrollment strategies, and mentors junior team members.

As a Senior Clinical Trial Manager, you will manage clinical trial operations, oversee budgets, develop monitoring plans, drive enrollment, and foster relationships with stakeholders.

The Clinical Research Associate will design and analyze clinical trials, ensuring protocol compliance, data integrity, and patient safety while collaborating with site staff and investigators.

The Clinical Systems Specialist will design and analyze clinical trials, interpret medical data, and support UAT processes within clinical systems.

Oversee and monitor clinical trial sites to ensure protocol, regulatory and GCP compliance; conduct site visits; manage multiple sites; ensure data integrity and participant safety; train and support site staff; collaborate with cross-functional teams and maintain stakeholder relationships.