Experteer OverviewIn this CRA role, you contribute to the development and oversight of drugs and medical devices by conducting site visits and ensuring compliance with protocols and regulations. You work within a team of therapeutic and regulatory experts to advance pharmaceutical and device development. The position emphasizes hands‐on training through the PACE program, broad exposure to multiple therapeutic areas, and opportunities for career growth. You will travel nationally and help improve trial conduct and data integrity in a dynamic environment.Retribuzione / BenefitsConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with approved protocolsCommunicate with site staff including coordinators and physiciansVerify investigator qualifications, training, resources, and facilitiesVerify source documentation and adherence to GCP, SOPs,



and regulatory requirementsEnsure eligible subject enrollment and review regulatory documentsMedical device and/or investigational product/drug accountability and inventoryReview adverse events and concomitant medications for accurate data reportingAssess site patient recruitment and retention and suggest improvementsComplete monitoring reports and follow‐up letters with findings and actionsResponsabilitàMaster degree in health‐related fieldWillingness to travel 60‐80% nationallyFamiliarity with Microsoft OfficeCRA certification completed per DMC 15/11/2011Fluent in English and ItalianStrong communication and presentation skills (a plus)Requisiti 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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📌 Research Associate (Italia)
🏢 Altro
📍 Italia