Jobs at ICON plc

As a Senior CRA, you will manage clinical trial activities ensuring compliance with protocols and standards, conduct site visits, train staff, and facilitate collaboration among teams.

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

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.

As a Senior CRA, you will manage early-phase oncology clinical trial activities ensuring compliance with protocols and regulatory standards, conducting site visits, training staff, and collaborating with teams for data accuracy.

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.

Monitor clinical trial sites, ensure adherence to protocols, conduct site visits, train staff, and manage relationships for oncology trials.

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

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

Clinical Trial Liaisons provide scientific support to clinical trial sites, optimize patient recruitment strategies, and engage with stakeholders to achieve trial goals. They require strong communication skills and a doctoral degree.

The Clinical Research Coordinator Nurse conducts clinical trial procedures, documents data, assists in patient recruitment, and collaborates with teams for compliance.

The Clinical Research Associate will monitor sites for compliance, manage documentation, ensure patient safety, facilitate training, and oversee drug accountability in oncology trials.

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.

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.

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 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.