I have a bachelor's degree in biomedicine, specialising in clinical analysis, and have been working in clinical research for over three years. I am currently a research analyst at a site, responsible for SSU and regulatory affairs, working on clinical studies in oncology, specialities and investigator-initiated studies. I provide support in responding to qualification visits and completing feasibility questionnaires. In addition, I am responsible for national coordination studies, providing support to participating sites in regulatory affairs.I have a diploma in professional training in clinical research from Invitare. I have great skills with the CEP/CONEP system (Brazil platform), ethical submissions and the documents required to initiate clinical studies.