I’m graduated cum lode in Biomolecular and Cellular Science (LM-6) at University of Ferrara. In April 2015 I attended the 40-hour "Missione CRA" at the CRO Yghea, in Bologna, a theoretical training of clinical monitors, in compliance with the Italian Ministerial Decree 15.11.2011, in order to learn the basic concepts of clinical research (on the 4th of February 2015 I also attended the course "Clinical Research for Beginners" at the Cro Yghea in Bologna, aimed at defining the GCP principles). Since june 2015 I work at the CRO Farmastudio-Fast in Rovigo. My responsibilities are focused on management of documents to start a clinical trial. Some of these are: - collect general information regarding local procedures of single site/Ethic Commette- preparation informed consents in according to sponsor SOP- submission essential documents at the Competent Authority and Ethics Committees - Follow-Up of the authorization process- contract negotiation - preparation Investigator Trial File- preparation SOPI’m a proactive, determinate and diplomatic person. I’m well organized, precise and goal oriented. I have a good communication skills and a strong predisposition to interpersonal relationships so I have no problem to work independently or as a part of team because I am friendly and I always available to help my colleagues if they need it.