pClinical Research Associate I (CRA I) – Italy /ppbr/ppbLocation: /b Italy /ppbWorking arrangement: /b Home-based with travel to clinical trial sites /ppbEmployment type: /b Full-time, permanent /ppbr/ppbThe Opportunity /b /ppWe are partnering with an international clinical research organisation seeking a Clinical Research Associate I to support clinical trials across Italy.
/ppThis 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.
/ppbr/ppbKey Responsibilities /b /pulliConduct site qualification, initiation, routine monitoring and close-out visits.
/liliMonitor assigned clinical trial sites in accordance with study protocols, ICH-GCP and applicable Italian and European regulations.
/liliReview source documentation and verify the accuracy and completeness of clinical trial data.
/liliEnsure investigator site files and essential study documentation remain complete, accurate and inspection-ready.
/liliSupport investigative sites with patient recruitment, data entry and query resolution.
/liliIdentify and escalate protocol deviations, compliance concerns and site-level risks.
/liliPrepare accurate monitoring visit reports and follow up on outstanding actions.
/liliBuild effective relationships with investigators, study coordinators and other site personnel.
/liliCollaborate with Clinical Trial Managers and wider international project teams.




/liliEnsure assigned sites meet agreed quality standards, recruitment objectives and study timelines.
/li /ulpbr/ppbCandidate Requirements /b /pulliPrevious experience within clinical research, ideally including exposure to clinical site monitoring.
/liliExperience as a Junior CRA, CRA I, In-House CRA, Clinical Trial Assistant or in a similar clinical research position.
/liliA good understanding of clinical trial processes and ICH-GCP requirements.
/liliA degree in life sciences, pharmacy, nursing, medicine or another relevant discipline.
/liliFluent Italian and strong professional English.
/liliCurrently based in Italy.
/liliWillingness and ability to travel regularly to investigative sites across Italy.
/liliStrong organisational, communication and report-writing skills.
/liliAbility to manage multiple priorities and work effectively with limited supervision.
/liliA valid driving licence is preferred.
/li /ulpbr/ppbWhy Consider This Opportunity?
/b /pulliDevelop your independent clinical monitoring experience.
/liliSupport clinical trials within an international CRO environment.
/liliWork closely with experienced clinical operations professionals.
/liliBenefit from ongoing training and professional development.
/liliBuild a long-term career within clinical research.
/li /ulpbr/ppIf you are based in Italy and would be interested in developing your career as a Clinical Research Associate, please apply or get in touch for a confidential discussion.
/p

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