Jobs at ICON plc

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

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 Senior Clinical Research Associate monitors clinical trials, ensures compliance with regulations, mentors junior staff, and maintains quality and integrity of studies.

As a Clinical Operations Study Lead at ICON, you'll manage projects, lead teams, develop project plans, and mentor staff to ensure successful project execution in clinical settings.

Senior Site Monitor responsible for planning and conducting on-site and remote monitoring across Phase I-IV studies. Ensures site compliance with protocol, data quality, and participant safety, conducts source data verification, manages site communications, supports RBQM processes, and participates in audits and inspections.

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

The Senior Issue Lead manages Major Quality Event investigations, coordinates audits, ensures compliance with GCP standards, and trains Issue Leads. This role involves root cause analysis, process improvement, and leading quality assessments.

Oversee and manage clinical trial activities, ensuring adherence to protocols and regulatory standards while leading monitoring tasks and site performance assessment.

The Third Party Quality Lead manages third-party quality risks in clinical operations, ensures GCP compliance, and oversees vendor performance and quality systems.

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 Quality ICM Issue Lead oversees quality event case management, leading investigations, notifications, root cause analysis, and process improvements within clinical development.

Responsible for monitoring cardiovascular medical device studies, ensuring compliance with FDA regulations, and fostering effective relationships with stakeholders.

Oversee cardiovascular clinical trials, ensuring compliance with regulations while managing site relationships and communication. Requires 3 years of monitoring experience and strong problem-solving skills.

The Senior Clinical Research Associate will monitor cardiovascular devices, ensuring compliance with FDA regulations and managing study communication, while travelling regionally up to 65%.

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 Global Study Lead, you will manage clinical trial aspects, focusing on budget oversight, study monitoring, enrollment, and stakeholder relations.

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.

The Senior Clinical Research Associate manages monitoring for cardiovascular clinical trials, ensuring compliance with FDA regulations and guiding teams to resolve site issues effectively.

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

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with sites; review data and support study documentation.