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 integral expertise and a strong, patient-focused mission.

Compensaciones / Beneficios

- 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 - barcelona
🏢 Icon Clinical
📍 Barcelona