14 set - Milano
Medpace
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
- 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
- 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
Requisiti fondamentali
- 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
- Strong communication skills
- Presentational abilities
- Team collaboration
- Microsoft Office
- Regulatory document review
- GCP/compliance knowledge
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