Experteer Overview

As a CRA II at ICON, you will design and analyse clinical trials and monitor study conduct to ensure data quality and patient safety. You will work closely with investigators and site staff to drive compliant trial execution in a fast-paced environment.

This role offers the opportunity to contribute to innovative therapies at a global CRO with a strong commitment to inclusion. You will travel as needed to sites and play a key part in shaping the clinical development program.

Compensaciones / Beneficios

- 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 the preparation and review of study documentation,



including protocols and clinical study reports

Responsabilidades

- 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 as required (approximately 60%)

Requisitos principales

- Various annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- General Employee Assistance Programme (Life Works)
- Life assurance
- Flexible country-specific benefits

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