Clinical Research Monitoring (CRA)

Our clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates to join our Clinical Monitoring team in Italy. This position will work with a team to accomplish tasks and projects that are instrumental to the company’s success. Medpace will provide comprehensive initial and ongoing training depending on your previous experience.

Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;

Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;

Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;

Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;

Regulatory document review;

Medical device and/or investigational product/drug accountability and inventory;

Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;

Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Master degree in health-related field;

Willing to travel up to 60-80% nationally;

Familiarity with Microsoft® Office;

Fluent in English and Italian language;

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

The work we do today will improve the lives of people living with illness and disease in the future.

Flexible work environment

Structured career paths with opportunities for professional growth

Employee health and wellness initiatives

Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility