Experienced Clinical Research Associate, Multi Sponsor

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