Experteer Overview

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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 / Ventajas
• 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 staff to facilitate smooth study conduct
• Perform data review and resolution of queries to maintain high-quality clinical data (unblinded CRF)




• Contribute to the 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 3 years of experience as a Clinical Research Associate
• Experience in Oncology Early Phase studies
• Dose escalation studies experience highly valued
• Unblinded studies experience highly valued
• In-depth knowledge of clinical trial processes, regulations, xqbhyrx 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
• Global Employee Assistance Programme LifeWorks
• Life assurance
• Flexible country-specific optional benefits

📌 CRA II (Madrid)
🏢 Icon Clinical
📍 Madrid