Experteer OverviewJoin Medpace as a Clinical Research Associate in Italy, working full-time from home or office with a Clinical Monitoring team. You will help ensure trials run in line with protocols, GCP, and regulatory standards, while collaborating with site staff and cross-functional teams. The role offers extensive training and opportunities to grow within a global CRO. You will contribute to patient recruitment, data integrity, and compliance, driving the success of clinical studies.Retribuzione / BenefitsPerform qualification, initiation, monitoring, and closeout visits at sites per the approved protocolCommunicate with site staff including coordinators and physiciansVerify investigator qualifications, training, facilities,



and resourcesVerify data and ensure good documentation practices and correct protocol deviationsEnsure eligible subject enrollment and conduct regulatory document reviewsManage medical device and/or investigational product accountability and inventoryReview adverse events and concomitant medications for accurate reportingAssess site recruitment/retention performance and suggest improvementsPrepare monitoring reports and follow-up letters summarizing findings and actions to ensure complianceResponsabilitàMaster degree in health-related fieldCRA certification completed as per DMC 15/11/2011Previous experience as CRAWillingness to travel up to 60-80% nationallyFamiliarity with Microsoft OfficeFluent in English and ItalianRequisiti fondamentaliFlexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiatives
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📌 Clinical Research Associate (Italia)
🏢 Altro
📍 Italia