Experienced Clinical Research Associate, Multi Sponsor

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