Overview 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.
Retribuzione / 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
Responsabilità
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
Requisiti fondamentali
Master in health-related field
CRA certification completed per DMC 15/11/2011
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
strong communication skills
presentation skills
team collaboration
Microsoft Office
Good documentation practices (GCP)
Regulatory document review

Clinical Research Monitor

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