Overview

As a Clinical Research Associate II at ICON, you will support the design, monitoring and analysis of clinical trials to advance innovative therapies. You will ensure protocol compliance, data integrity and patient safety while collaborating with investigators and site staff. Your work helps maintain high-quality data and documentation for study reports. This role offers exposure to global trials and a fast-paced, cross-functional environment that values inclusive, high-performance teams.

Compensaciones / Beneficios Annual leave entitlements

Health insurance offerings

Retirement planning offerings

General Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Responsabilidades Conduct site qualification, initiation, monitoring and close-out visits for trials

Ensure protocol compliance, data integrity and patient safety throughout the trial

Collaborate with investigators and site staff to facilitate study conduct





Perform data review and resolve 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

Knowledge of clinical trial processes, regulations and ICH-GCP guidelines

Strong organizational and communication skills, attention to detail

Ability to work independently and collaboratively in a fast-paced environment

Ability to travel at least 60% of the time with a valid driver's license

Good level of English

Strong communication

Attention to detail

Team collaboration

Clinical trial processes

ICH-GCP knowledge

Data query resolution

📌 CRA 2 (Barcelona)
🏢 Icon Clinical
📍 Barcelona