Overview As a Clinical Research Associate II at ICON, you contribute to designing and analyzing clinical trials and interpreting medical data to advance innovative therapies. You will oversee site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity, and patient safety. You will collaborate with investigators and site staff and support data review and study documentation. This role combines independent work with cross-functional teamwork to sustain trial quality and impact.
Compensaciones / Beneficios Annual leave entitlements
Health insurance offerings
Retirement planning offerings
Integral Employee Assistance Programme (TELUS Health)
Life assurance
Flexible country-specific benefits
Responsabilidades 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
Requisitos principales Bachelors 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
Ability to travel at least 60% of the time (international and domestic) and a valid driver's license
Good level of English
Strong organizational skills
Effective communication
Attention to detail
Independent and collaborative work style
Knowledge of clinical trial processes and ICH-GCP guidelines
Data review and query resolution

📌 Clinical Trial Assistant (Barcelona)
🏢 Icon Clinical
📍 Barcelona