Experteer Overview
As a CRA II at ICON, you design and analyze clinical trials to advance innovative therapies. You work within a collaborative, values-driven team to ensure protocol adherence, data integrity, and patient safety across trial lifecycles. You will monitor sites, review data, and contribute to study documentation, partnering with investigators to enable high-quality study conduct. This role offers the chance to impact patient access to new medicines while working in a fast-paced, globally distributed environment.

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 investigators and site staff to facilitate smooth study conduct
• Perform data review and resolution of queries to maintain high-quality clinical data




• Contribute to preparation and review of study documentation, including protocols and clinical study reports

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

Requisitos principales
• Various annual leave entitlements
• Health insurance offerings
• Competitive retirement planning
• General Employee Assistance Programme LifeWorks
• Life assurance
• Flexible country-specific optional benefits

📌 CRA 2 o SCRA (Madrid)
🏢 Icon Clinical
📍 Madrid