Experteer Overview
As a CRA II at ICON Strategic Solutions, you will drive the monitoring and analysis of clinical trials within a sponsor-dedicated model. You will work with investigators and sites to ensure protocol adherence, data integrity, and patient safety while contributing to study documentation and regulatory compliance. This role blends independent execution with cross-functional collaboration to support the development of innovative therapies at scale. You will engage in meaningful trials that impact patient care and benefit from ICON’s general expertise and supportive culture.

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 resolve 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
• Annual leave entitlements
• Health insurance offerings
• Competitive retirement planning
• Global Employee Assistance Programme LifeWorks
• Life assurance
• Flexible country-specific benefits

📌 Clinical Research Associate 2 (Madrid)
🏢 Icon Clinical
📍 Madrid