Clinical Research Associate I (CRA I) – Italy
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Location:
Italy
Working arrangement:
Home-based with travel to clinical trial sites
Employment type:
Full-time, permanent
The Opportunity
We are partnering with an international clinical research organisation seeking a Clinical Research Associate I to support clinical trials across Italy.
This opportunity would suit an early-career CRA who has gained initial clinical research or monitoring experience and is now looking to develop their independent site-management capabilities within an international CRO environment.
Key Responsibilities
Conduct site qualification, initiation, routine monitoring and close-out visits.
Monitor assigned clinical trial sites in accordance with study protocols, ICH-GCP and applicable Italian and European regulations.
Review source documentation and verify the accuracy and completeness of clinical trial data.




Ensure investigator site files and essential study documentation remain complete, accurate and inspection-ready.
Support investigative sites with patient recruitment, data entry and query resolution.
Identify and escalate protocol deviations, compliance concerns and site-level risks.
Prepare accurate monitoring visit reports and follow up on outstanding actions.
Build effective relationships with investigators, study coordinators and other site personnel.
Collaborate with Clinical Trial Managers and wider international project teams.
Ensure assigned sites meet agreed quality standards, recruitment objectives and study timelines.
Candidate Requirements
Previous experience within clinical research, ideally including exposure to clinical site monitoring.
Experience as a Junior CRA, CRA I, In-House CRA, Clinical Trial Assistant or in a similar clinical research position.
A good understanding of clinical trial processes and ICH-GCP requirements.
A degree in l

📌 Clinical Research Associate I (Castagnole Piemonte)
🏢 Warman O'Brien
📍 Castagnole Piemonte