Overview
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As a Clinical Research Associate II at ICON, you will support the design, monitoring and analysis of clinical trials to advance innovative therapies. You will ensure protocol compliance, data integrity and patient safety while collaborating with investigators and site staff. Your work helps maintain high-quality data and documentation for study reports. This role offers exposure to global trials and a fast-paced, cross-functional environment that values inclusive, high-performance teams.
Compensaciones / Beneficios
Annual leave entitlements
Health insurance offerings
Retirement planning offerings
Integral Employee Assistance Programme
Life assurance
Flexible country-specific benefits
Responsabilidades
Conduct site qualification, initiation, monitoring and close-out visits for trials
Ensure protocol compliance, data integrity and patient safety throughout the trial




Collaborate with investigators and site staff to facilitate 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
Requisitos principales
Bachelors degree in a scientific or healthcare-related field
Minimum of 2 years of experience as a Clinical Research Associate
Knowledge of clinical xqbhyrx trial processes, regulations and ICH-GCP guidelines
Strong organizational and communication skills, attention to detail
Ability to work independently and collaboratively in a fast-paced environment
Ability to travel at least 60% of the time with a valid driver’s license
Good level of English
Strong communication
Attention to detail
Team collaboration
Clinical trial processes
ICH-GCP knowledge
Data query resolution

📌 CRA 2 (Barcelona)
🏢 Icon Clinical
📍 Barcelona