Clinical Research Associate – Site Monitoring
CTI Clinical Trial and Consulting Services in Italy seeks a Clinical Research Associate to serve as main CTI contact for assigned study sites and to conduct monitoring visits in line with ICH-GCP. You will support start-up activities, manage essential regulatory documents, participate in team meetings, and help ensure accurate IP storage and trial materials. Fluent English is required; a life science background is preferred. #J-18808-Ljbffr