Experteer Overview In this CRA role, you contribute to the development and oversight of drugs and medical devices by conducting site visits and ensuring compliance with protocols and regulations. You work within a team of therapeutic and regulatory experts to advance pharmaceutical and device development. The position emphasizes hands?on training through the PACE program, broad exposure to multiple therapeutic areas, and opportunities for career growth. You will travel nationally and help improve trial conduct and data integrity in a dynamic environment.
Retribuzione / Benefits Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with approved protocols
Communicate with site staff including coordinators and physicians
Verify investigator qualifications, training, resources, and facilities
Verify source documentation and adherence to GCP, SOPs, and regulatory requirements
Ensure eligible subject enrollment and review regulatory documents




Medical device and/or investigational product/drug accountability and inventory
Review adverse events and concomitant medications for accurate data reporting
Assess site patient recruitment and retention and suggest improvements
Complete monitoring reports and follow?up letters with findings and actions
Responsabilità Master degree in health?related field
Willingness to travel *****% nationally
Familiarity with Microsoft Office
CRA certification completed per DMC 15/11/2011
Fluent in English and Italian
Strong communication and presentation skills (a plus)
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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📌 Clinical Research Associate (Bardi)
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