In this full-time role, you join Medpace's Clinical Monitoring team to support site-based trials in Italy, helping advance clinical development for diverse therapies. You will perform monitoring visits, ensure protocol and regulatory compliance, and contribute to data integrity and site performance. The position offers comprehensive training and a clear path for professional growth within a global CRO. Your work will directly impact trial quality, patient safety, and timely study delivery.

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 per the approved protocol

Coordinate with site staff including coordinators and physicians

Verify investigator qualifications, training, facilities, laboratories, equipment, and staff





Perform source data verification and ensure good documentation practices (GCP/SOPs) and report protocol deviations

Confirm eligibility of enrolled subjects and perform regulatory document reviews

Oversee medical device and/or investigational product/drug accountability and inventory

Review adverse events and related data for accurate reporting

Assess site recruitment and retention performance and suggest improvements

Prepare monitoring reports and follow-up letters with actionable recommendations

Master in health-related field

Previous experience as CRA

Willingness to travel 60-80% nationally

Familiarity with Microsoft Office

Fluent in English and Italian

Strong communication and presentation skills would be considered a plus team collaboration

Microsoft Office

Good documentation practices (GCP)

Regulatory document review

Experienced Clinical Research Associate, Multi Sponsor varese, lombardia, it

📌 Experienced Clinical Research Associate, Multi Sponsor (Varese)
🏢 Altro
📍 Varese