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.

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

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

Master degree in health-related field

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

Cross-functional collaboration (implied)

Microsoft Office

Regulatory knowledge (GCP and SOPs)

Data verification against case report forms

Experienced Clinical Research Associate (Cra)

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