Clinical Research Associate

Overview

In this CRA role at Medpace you will support the integrity of clinical studies across pharmaceutical and medical device development. You'll join a training-focused program (PACE) that accelerates your skills toward independent CRA responsibilities. You work across sites, regulators, and cross-functional teams to ensure compliant trials and data quality, with substantial travel. This position offers structured growth, exposure to multiple therapeutic areas, and a mission-driven environment that aims to improve patient outcomes. You'll be part of a supportive CRO with clear promotion paths and ongoing professional development.

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 at research sites per protocol and SOPs
• Communicate with site staff including coordinators and physicians
• Verify investigator qualifications, training, resources, facilities, labs, equipment, and staff
• Verify source documentation and maintain good documentation practices; handle protocol deviations
• Ensure enrollment of eligible subjects and perform regulatory document reviews
• Monitor adverse events and accurate data reporting per protocol
• Assess site recruitment and retention and suggest improvements
• Prepare monitoring reports and follow-up letters with significant findings and recommended actions

Requisiti fondamentali

• Master degree in health-related field
• Willingness to travel 60-80% nationally
• Familiarity with Microsoft Office
• CRA certification completed as per DMC 15/11/2011
• Fluent in English and Italian
• Strong communication and presentation skills a plus
• strong communication
• presentation skills
• team collaboration
• Microsoft Office
• CRA certification
• GCP and regulatory compliance knowledge