ppAre you an experienced Clinical Research Associate looking to join a dynamic and growing clinical research organisation? /p pWe are seeking a CRA II to manage investigative sites across Italy, ensuring clinical trials are conducted in accordance with study protocols, ICH-GCP, and applicable regulatory requirements. /p h3Key Responsibilities /h3 ul liConduct site qualification, initiation, monitoring, and close-out visits. /li liEnsure patient safety, data integrity, and protocol compliance. /li liPerform source data verification and review study documentation. /li liManage site relationships and provide ongoing support to investigators and study staff. /li liAssist with ethics committee and regulatory submissions where required. /li liMonitor investigational product accountability and site performance. /li liMaintain Trial Master File (TMF) documentation and support query resolution. /li liCollaborate with cross-functional study teams to ensure successful trial delivery.



/li /ul h3About You /h3 ul liLife Sciences degree or equivalent experience, plus recognised CRA training. /li liMinimum 4 years' clinical research experience. /li liMinimum 2 years' monitoring experience as a CRA. /li liStrong knowledge of ICH-GCP, clinical trial regulations, and site management. /li liFluent in Italian with a good command of English. /li liExcellent communication, organisation, and problem-solving skills. /li liAbility to work independently and manage multiple priorities. /li liValid driver's licence and willingness to travel up to 75%. /li /ul h3What We Offer /h3 ul liHome-based flexibility. /li liOpportunity to work on international clinical trials. /li liCollaborative and supportive team environment. /li liCompetitive salary and benefits package. /li /ul /p #J-18808-Ljbffr

📌 Clinical Research Associate II (Italia)
🏢 Linical
📍 Italia