CRA II

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ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values‑driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What You Will Be Doing

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- 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

Your profile

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- 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.
- Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What ICON Can Offer You
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurt

📌 Senior CRA (Romano di Lombardia)
🏢 ICON San Antonio
📍 Romano di Lombardia