15 ott - Monza
Medpace
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 * C
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