22 set - Pavia
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 CRA certification GCP and regulatory compliance knowledge
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Snai
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Kpmg Italy