Jobs at ICON plc

As a Senior Clinical Research Associate, you will oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements while managing site performance and collaborating with cross-functional teams.

As a Clinical Technology Specialist, you will lead the design and implementation of clinical systems, managing operations and ensuring compliance with regulations.

The Senior Biostatistician I will lead early phase clinical trials, provide statistical inputs for protocols and reports, and mentor junior statisticians.

The Lead CRA manages clinical trial sites, ensures compliance with regulations, mentors CRAs, and oversees data integrity. Responsibilities include site management, issue resolution, and collaboration with cross-functional teams.

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

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.

The Lead Clinical Research Associate oversees clinical trial sites, ensuring compliance with regulations and study protocols, mentoring CRAs, and ensuring data integrity and patient safety.

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 will manage site activities and ensure compliance during Oncology clinical trials, focusing on data integrity and subject safety.

As a Senior Clinical Research Associate, you will monitor clinical trial sites, ensure protocol compliance, conduct site visits, and provide training and support to staff.

As a Senior Clinical Research Associate, you will monitor clinical trials, ensure compliance with protocols, support site staff, and maintain data integrity.

The Senior Clinical Research Associate will manage clinical trials, ensure adherence to protocols, conduct site visits, and provide training to maintain standards.

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.