Experteer Overview In this role you join Medpace's Clinical Monitoring team in Italy to perform site-based monitoring activities for clinical studies. You will receive comprehensive training and work either remotely or from an office, contributing to study integrity and regulatory compliance. You collaborate with site staff and cross-functional teams to ensure quality data and patient safety, with opportunities for career growth in a global CRO. This position offers meaningful impact by supporting efficient, compliant clinical development.
Retribuzione / Benefits Conduct qualification, initiation, monitoring and closeout visits at research sites per protocol
Communicate with site staff, coordinators and clinical research physicians
Verify investigator qualifications, training, facilities and resources
Verify data through source documentation checks and ensure good documentation practices
Ensure eligibility of enrolled subjects and perform regulatory document review




Manage regulatory documents and accountability for investigational products/devices
Review adverse events and related data to ensure accurate reporting
Assess site patient recruitment/retention and suggest improvements
Prepare monitoring reports and follow-up letters summarizing findings and recommended actions
Responsabilità Master degree in health-related field
CRA certification completed per DMC 15/11/2011
Previous experience as CRA
Willingness to travel 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 events
Employee health and wellness initiatives #J-18808-Ljbffr

📌 Clinical Research Associate (Italia)
🏢 Experteer Italy
📍 Italia