CRA II

Icon Clinical PLC · madrid, madrid, Spain

Location
madrid
Job Type
Full-time
Posted
July 13, 2026

Job Description

Experteer Overview
¿Todo listo para enviar su solicitud? Por favor, lea la descripción al menos una vez antes de hacer clic en Solicitar.
In this role you contribute to clinical trial monitoring within ICON, driving data integrity and patient safety across oncology studies. You will work closely with cross-functional teams to support trial conduct, from site qualification to close-out, and contribute to essential study documentation. The position offers exposure to unblinded data management and early-phase dose-escalation studies, shaping the execution of innovative therapies. You’ll operate in a fast-paced environment with significant travel, making a meaningful impact on trial quality and patient outcomes.
Compensaciones / Beneficios
• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborate with the pharmacy team and site ...

Ready to Apply?

Submit your application for CRA II at Icon Clinical PLC

Apply Now