Clinical Research Associate II - Italy
At Linical · Milan, Italy
- Operations
Where you can work from
Open to Italy
“Milan, Italy”
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- Posted
- 28 August 2026
- First seen by us
- 12 October 2026
- Last checked
- 5 hours ago
Job description
From Linical’s job post, as they wrote it.
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.
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* 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.
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