Experienced Clinical Research Associate (Cra)

pIn 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. /pulliFlexible work environment /liliCompetitive compensation and benefits package /liliCompetitive PTO packages /liliStructured career paths with opportunities for professional growth /liliCompany-sponsored employee appreciation events /liliEmployee health and wellness initiatives /liliConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol /liliCommunicate with site staff including coordinators and investigators to ensure alignment and adherence to SOPs, GCP, and regulatory requirements /liliVerify investigator qualifications, training, facilities, laboratories, equipment, and staff /liliVerify source data against case report forms; ensure proper documentation and communicate protocol deviations /liliConfirm eligibility of enrolled subjects and perform regulatory document review /liliOversee medical device/investigational product/drug accountability and inventory /liliAssess and verify adverse events and related data for accurate reporting /liliEvaluate patient recruitment and retention performance and suggest improvements /liliPrepare monitoring reports and follow-up letters with findings and corrective actions /liliMaster degree in health-related field /liliPrevious experience as CRA /liliWillingness to travel up to 60-80% nationally /liliFamiliarity with Microsoft Office /liliFluent in English and Italian /liliStrong communication and presentation skills would be considered a plus /liliCross-functional collaboration (implied) /liliMicrosoft Office /liliRegulatory knowledge (GCP and SOPs) /liliData verification against case report forms /li /ul #J-18808-Ljbffr