Agnese Corbetta

Background

About Agnese Corbetta

Senior Regulatory Officer at PSI CRO, I am focused on the management of the regulatory aspects of clinical trials throughout their whole lifecycle, in Europe and worldwide. In my role as Regulatory Lead, I coordinate the work of the local regulatory groups of each country and I directly manage the application dossiers in the European portal CTIS. Every study I get my hands on brings different layers of complexity (from management of a diverse geomix to specific trial features, such as gene therapy or pediatric population, from technicalities of the CTIS portal to mentoring junior colleagues) and I see each challenge as a precious opportunity to grow and learn. My journey in clinical research began soon after graduating in medical biotechnology, when I felt that my work at the bench, albeit fundamental, was too distant from patients. After turning down a PhD opportunity at Heidelberg University, Germany, I entered PSI CRO as Clinical Trial Administrator. My first year in PSI proved to be the perfect opportunity to see clinical trials from Clinical Operations and StartUp perspectives, a background that proves useful still today. Interest then led me to the Regulatory Department, where over time I grew from supportive Regulatory Affairs Assistant helping with submissions in Italy to independent Senior Regulatory Officer with a global role.