Experteer Overview In 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.
Responsibilities Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol
Communicate with site staff including coordinators and investigators to ensure alignment and adherence to SOPs, GCP, and regulatory requirements
Verify investigator qualifications, training, facilities, laboratories, equipment, and staff
Verify source data against case report forms; ensure proper documentation and communicate protocol deviations

Confirm eligibility of enrolled subjects and perform regulatory document review
Oversee medical device/investigational product/drug accountability and inventory
Assess and verify adverse events and related data for accurate reporting
Evaluate patient recruitment and retention performance and suggest improvements
Prepare monitoring reports and follow-up letters with findings and corrective actions
Qualifications Master degree in health-related field
CRA certification completed per DMC 15/11/2011
Previous experience as CRA
Willingness to travel up to 60-80% nationally
Familiarity with Microsoft Office
Fluent in English and Italian
Strong communication and presentation skills would be considered a plus
Benefits Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives

Experienced Clinical Research Associate

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