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

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

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.

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

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

The Clinical Research Associate will manage clinical trial processes including site visits, data integrity, and prepare study documentation to ensure compliance and patient safety.

The Clinical Research Associate will manage clinical trials, ensure compliance and data integrity, and collaborate with site staff and investigators.

As a Clinical Research Associate, you'll conduct clinical trials, ensuring protocol compliance and data integrity while collaborating with site staff and investigators.

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