Are you an experienced Clinical Research Associate looking to join a dynamic and growing clinical research organisation?

We are seeking a CRA II to manage investigative sites across Italy, ensuring clinical trials are conducted in accordance with study protocols, ICH-GCP, and applicable regulatory requirements.

Key Responsibilities

- Conduct site qualification, initiation, monitoring, and close-out visits.

- Ensure patient safety, data integrity, and protocol compliance.

- Perform source data verification and review study documentation.

- Manage site relationships and provide ongoing support to investigators and study staff.

- Assist with ethics committee and regulatory submissions where required.

- Monitor investigational product accountability and site performance.

- Maintain Trial Master File (TMF) documentation and support query resolution.

- Collaborate with cross-functional study teams to ensure successful trial delivery.





About You

- Life Sciences degree or equivalent experience, plus recognised CRA training.

- Minimum 4 years' clinical research experience.

- Minimum 2 years' monitoring experience as a CRA.

- Strong knowledge of ICH-GCP, clinical trial regulations, and site management.

- Fluent in Italian with a good command of English.

- Excellent communication, organisation, and problem-solving skills.

- Ability to work independently and manage multiple priorities.

- Valid driver's licence and willingness to travel up to 75%.

What We Offer

- Home-based flexibility.

- Opportunity to work on international clinical trials.

- Collaborative and supportive team environment.

- Competitive salary and benefits package.

📌 Clinical Research Associate II - Italy (Milano)
🏢 Linical
📍 Milano