Overview In this CRA II role, you support sponsor-driven clinical trials from a global, collaborative CRO. You will monitor sites, ensure data integrity and patient safety, and work with investigators to enable compliant study conduct. The position emphasizes independent yet cross-functional collaboration within a fast-paced environment. You contribute to study documentation and data review, helping advance novel therapies for patients worldwide. This home-based role in Barcelona offers development within ICON’s global expertise and a strong, patient-focused mission.

Compensaciones / Incentivos

competitive base salary performance related incentives health and wellbeing programmes including medical, dental, and vision coverage retirement and pension plans life assurance and disability coverage learning and development opportunities

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 study conduct Perform data review and resolution of queries to maintain high-quality clinical data Assist in preparation and review of study documentation, including protocols and clinical study reports

Requisitos principales

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 approximately 60% organizational skills communication skills attention to detail ICH-GCP knowledge clinical trial processes site monitoring and data review

📌 Clinical Research Associate - Icon Clinical PLC (Barcelona)
🏢 Icon Clinical
📍 Barcelona