Experteer Overview
In this role you design and analyze clinical trials, monitor sites, and ensure data integrity and patient safety. You work closely with investigators to drive compliant study conduct and contribute to study documentation. The position combines independent work with cross-functional collaboration in a fast-paced environment. This is an opportunity to impact innovative therapies while supporting ICON's mission to shape the future of clinical development.

Compensaciones / Beneficios
• Conduct site qualification, initiation, monitoring, and close-out visits
• Ensure protocol compliance, data integrity, and patient safety throughout trials
• Collaborate with investigators and site staff to facilitate study conduct
• Perform data review and resolve queries to maintain high-quality data
• Assist in preparation and review of study documentation, including protocols and CSRs





Responsabilidades
• Bachelor in Science in a scientific or healthcare-related field
• Minimum of 2 years as a Clinical Research Associate
• Strong knowledge of clinical trial processes, regulations, and ICH-GCP
• Excellent organizational and communication skills with attention to detail
• Ability to work independently and collaboratively in a fast-paced environment
• Willingness to travel approximately 60%

Requisitos principales
• annual leave entitlements
• health insurance offerings
• retirement planning offerings
• General Employee Assistance Programme (LifeWorks)
• life assurance
• flexible country-specific optional benefits

📌 Clinical Research Associate (Barcelona)
🏢 Icon Clinical
📍 Barcelona