ppClinical Research Associate I (CRA I) – Italy /p pLocation: Italy /p pWorking arrangement: Home-based with travel to clinical trial sites /p pEmployment type: Full-time, permanent /p h3The Opportunity /h3 pWe are partnering with an international clinical research organisation seeking a Clinical Research Associate I to support clinical trials across Italy.
/p pThis 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.
/p h3Key Responsibilities /h3 ul liConduct site qualification, initiation, routine monitoring and close-out visits.
/li liMonitor assigned clinical trial sites in accordance with study protocols, ICH-GCP and applicable Italian and European regulations.
/li liReview source documentation and verify the accuracy and completeness of clinical trial data.
/li liEnsure investigator site files and essential study documentation remain complete, accurate and inspection-ready.
/li liSupport investigative sites with patient recruitment, data entry and query resolution.
/li liIdentify and escalation protocol deviations, compliance concerns and site-level risks.
/li liPrepare accurate monitoring visit reports and follow up on outstanding actions.
/li liBuild effective relationships with investigators, study coordinators and other site personnel.




/li liCollaborate with Clinical Trial Managers and wider international project teams.
/li liEnsure assigned sites meet agreed quality standards, recruitment objectives and study timelines.
/li /ul h3Candidate Requirements /h3 ul liPrevious experience within clinical research, ideally including exposure to clinical site monitoring.
/li liExperience as a Junior CRA, CRA I, In-House CRA, Clinical Trial Assistant or in a similar clinical research position.
/li liA good understanding of clinical trial processes and ICH-GCP requirements.
/li liA degree in life sciences, pharmacy, nursing, medicine or another relevant discipline.
/li liFluent Italian and strong professional English.
/li liCurrently based in Italy.
/li liWillingness and ability to travel regularly to investigative sites across Italy.
/li liStrong organisational, communication and report-writing skills.
/li liAbility to manage multiple priorities and work effectively with limited supervision.
/li liA valid driving licence is preferred.
/li /ul h3Why Consider This Opportunity?
/h3 ul liDevelop your independent clinical monitoring experience.
/li liSupport clinical trials within an international CRO environment.
/li liWork closely with experienced clinical operations professionals.
/li liVantaggi from ongoing training and professional development.
/li liBuild a long-term career within clinical research.
/li /ul /p #J-*****-Ljbffr

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