Experteer Overview

As a CRA II at ICON, you will support the design and analysis of clinical trials, translating complex data into actionable insights. You will conduct site visits and monitor progress to ensure patient safety, data integrity, and protocol adherence.

You’ll work with investigators and site staff to enable smooth study conduct in a fast-paced environment. This role offers meaningful impact in advancing innovative therapies and shaping the future of clinical development.

Compensaciones / Ventajas

- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
- Collaborating with investigators and site staff to facilitate smooth study conduct
- Performing data review and resolution of queries to maintain high-quality clinical data




- Contributing 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 approximately 60%

Requisitos principales

- Annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- Global Employee Assistance Programme Life Works
- Life assurance
- Flexible country-specific benefits

📌 Cra ii (Madrid)
🏢 Icon Clinical
📍 Madrid