Overview

As a Clinical Research Associate II, you will support sponsor-dedicated trials and contribute to the design, monitoring, and analysis of clinical studies. You will ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and study teams. This role offers general exposure within ICON’s extensive sponsor network and opportunities to advance trials that benefit patients worldwide. You will drive quality through data review, documentation, and cross-functional coordination.

Compensaciones / Beneficios

- Competitive base salary
- Performance-related incentives
- Health and wellbeing programmes
- 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 smooth 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

- 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%

- Strong organizational skills
- Clear communication
- Attention to detail
- Clinical trial processes
- ICH-GCP guidelines
- Data review and query resolution

📌 CRA - Barcelona Barcelona
🏢 Icon Clinical
📍 Barcelona