Clinical Research Associate I

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/800dfo

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-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/800dfo