Clinical Research Associate
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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
- 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
- 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
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