Clinical Research Associate I
Pubblicato il 17-09-2026 - Warman O'Brien in Caserta
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