Experienced Clinical Research Associate, Home based

Experteer Overview

Join Medpace as a Clinical Research Associate in Italy, working full-time from home or office with a Clinical Monitoring team. You will help ensure trials run in line with protocols, GCP, and regulatory standards, while collaborating with site staff and cross-functional teams. The role offers extensive training and opportunities to grow within a global CRO. You will contribute to patient recruitment, data integrity, and compliance, driving the success of clinical studies.

Retribuzione / Benefits

• Perform qualification, initiation, monitoring, and closeout visits at sites per the approved protocol
• Communicate with site staff including coordinators and physicians
• Verify investigator qualifications, training, facilities, and resources
• Verify data and ensure good documentation practices and correct protocol deviations
• Ensure eligible subject enrollment and conduct regulatory document reviews
• Manage medical device and/or investigational product accountability and inventory
• Review adverse events and concomitant medications for accurate reporting
• Assess site recruitment/retention performance and suggest improvements
• Prepare monitoring reports and follow-up letters summarizing findings and actions to ensure compliance

Responsabilità

• Master degree in health-related field
• CRA certification completed as 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

Requisiti fondamentali

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation eventsEmployee health and wellness initiatives