Overview
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As a CRA II at ICON, you monitor and support clinical trials to ensure quality, compliance, and patient safety. You will work with investigators and site staff to drive study conduct and data integrity, contributing to study documentation and reports. This home-based role in Barcelona offers meaningful exposure to cutting-edge therapies within a collaborative, values-driven environment. You will leverage your trial experience to advance treatments and new medicines for patients.
Compensaciones / Ventajas
Competitive base salary
Health and wellbeing programmes
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
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 smooth study conduct
Perform data review and resolution of 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 xqbhyrx 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%)
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
strong organizational skills
excellent communication
attention to detail
clinical trial processes
regulations
ICH-GCP guidelines

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