Experteer Overview In this role you will contribute to the growth of our clinical monitoring activities in Italy as part of a collaborative team. You will conduct site visits, verify qualifications and resources, and ensure data quality and regulatory compliance. You will work across protocol-driven processes, training, and site communications to support safe and efficient trials. This position offers comprehensive training and opportunities to advance your career within a globally recognized CRO. You will be part of a mission-driven organization accelerating the development of medical therapeutics.
Retribuzione / Benefits Conduct qualification, initiation, monitoring, and closeout visits at research sites per protocol
Coordinate with site staff, CR physicians, and coordinators
Verify investigator qualifications, training, resources, facilities, and staff
Verify documentation and ensure GCP, SOP, and regulatory adherence with protocol deviations communicated
Ensure investigator enrolls only eligible subjects
Regulatory document review




Medical device and/or investigational product/drug accountability
Verify adverse events, SAEs, concomitant medications, and related illnesses data accuracy
Assess site recruitment and retention performance and suggest improvements
Prepare monitoring reports and follow-up letters with findings and recommended actions
Responsabilità Master degree in health-related field
CRA certification completed as per DMC 15/11/2011
Previous experience as CRA
Willing to travel up to 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
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📌 Experienced Clinical Research Associate, Multi Sponsor (Italia)
🏢 Altro
📍 Italia