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The Principal Auditor in CRQA ensures quality and compliance of clinical trials, manages client relationships, and supports governance and risk management activities.

As a Clinical Research Nurse at ICON, you will provide clinical care to research participants, administer products, monitor safety, document data, and partner with healthcare professionals to ensure compliance.

The Project Manager II will manage client relationships and oversee clinical laboratory studies, ensuring proper protocols and timelines are followed. Responsibilities include project management, budget oversight, and client communication.

Responsible for clinical trial monitoring, ensuring compliance, data integrity, and patient safety. Involves site visits and collaboration with investigators.

As a Senior CRA, you will monitor clinical trial sites, ensure compliance with regulations, manage site performance, and train staff to maintain trial standards.

The Lab Analyst I conducts laboratory tests for clinical research, ensuring quality control, data accuracy, and protocol adherence, while operating laboratory equipment.

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.

As a Clinical Research Associate II/Senior CRA, you will manage clinical trial processes, ensuring compliance, data integrity, and coordinating with site staff.

As a Senior Clinical Editor at ICON, you will edit and proofread scientific documents and publications, collaborate with medical writers, ensure regulatory compliance, mentor junior staff, and uphold quality standards in clinical content.

The Clinical Trial Liaison will design and analyze clinical trials, interpret medical data, and enhance patient recruitment and retention while collaborating with cross-functional teams.