Jobs at ICON plc

Lead oncology clinical trial monitoring, ensuring protocol, regulatory and GCP compliance. Conduct site visits, resolve issues, train and mentor site staff and CRAs, manage multiple sites, collaborate with cross-functional teams, maintain data integrity, and travel approximately 60% to support trial execution.

The Senior Director of Finance will oversee group accounting, ensure compliance with US GAAP and IFRS, provide strategic guidance, and lead complex accounting issues for ICON plc.

Lead onsite and remote monitoring for oncology clinical trials, ensuring data integrity, subject safety, TMF reconciliation, regulatory readiness, site activation, training, KRI monitoring, CAPA implementation, and site relationship management.

The Clinical Site Associate supports clinical trial operations, manages site communications, maintains documentation, and ensures compliance for site readiness.

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

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

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

Support and coordinate clinical trial site monitoring to ensure protocol, regulatory, and GCP compliance; prepare and review regulatory documents; collaborate with cross-functional teams; track site performance and report findings; mentor junior staff and support training initiatives.

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.

As a Senior Clinical Research Associate, you will manage clinical trials, ensuring protocol compliance, data integrity, and patient safety, while collaborating with site staff and preparing study documentation.

As a Clinical Research Associate, you will monitor clinical trials, ensuring adherence to protocols and regulations, conduct site visits, and train staff.

Lead data-driven feasibility and site strategy for clinical studies: assess protocol feasibility, build enrollment projections and scenario models, optimize country/site selection, coordinate global site intelligence, and provide strategic recommendations to improve recruitment timelines and study start-up efficiency.

As a Clinical Research Associate, you will monitor clinical trials, ensuring compliance and data integrity, while collaborating with site staff and investigators.

The Clinical Research Associate will conduct monitoring visits, ensure protocol compliance, collaborate with site staff, and maintain data integrity.

As a Global Study Manager, you will lead projects, manage cross-functional teams, and ensure successful project execution while mentoring team members.

Lead and manage end-to-end clinical trial site start-up and activation activities. Oversee site identification, feasibility, regulatory submissions, timelines, budgets, and risks. Mentor and lead a study start-up team, collaborate with sponsors and internal stakeholders, and drive process improvements to optimize start-up efficiency and compliance.

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

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