Overview

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 / Incentivos

- 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

- 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%)
- 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