Experienced Clinical Research Associate
Pubblicato il 21-09-2026 - Medpace in Varese
OverviewIn this role you join Medpace's Clinical Monitoring team in Italy to perform site monitoring, qualification, initiation, and closeout visits while ensuring protocol and regulatory compliance. You will verify investigator qualifications, manage data integrity, and support site performance to drive successful clinical trials. Travel up to 60-80% nationwide is required, with comprehensive training provided. This position offers growth within a global CRO focused on Phase I–IV development and diverse therapeutic areas.Retribuzione / BenefitsFlexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesResponsabilitàConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocolCommunicate with site staff including coordinators and investigators to ensure alignment and adherence to SOPs, GCP, and regulatory requirementsVerify investigator qualifications, training, facilities, laboratories, equipment,
and staffVerify source data against case report forms; ensure proper documentation and communicate protocol deviationsConfirm eligibility of enrolled subjects and perform regulatory document reviewOversee medical device/investigational product/drug accountability and inventoryAssess and verify adverse events and related data for accurate reportingEvaluate patient recruitment and retention performance and suggest improvementsPrepare monitoring reports and follow-up letters with findings and corrective actionsRequisiti fondamentaliMaster degree in health-related fieldCRA certification completed per DMC 15/11/2011Previous experience as CRAWillingness to travel up to 60-80% nationallyFamiliarity with Microsoft OfficeFluent in English and ItalianStrong communication and presentation skills would be considered a plusStrong communication skillsPresentation skillsCross-functional collaboration (implied)Microsoft OfficeRegulatory knowledge (GCP and SOPs)Data verification against case report forms