Hello, welcome!I have excellent experience in the areas of Clinical Research and Regulatory Affairs, working in the delegation of teams in studies, organization of documentation and data flows in accordance with best practices and legal requirements, monitoring of contract processes, training of teams involved, participation from qualification to completion of studies.- Ensuring compliance with the protocols of the Research Ethics Committee, drafting and updating SOPs focused on continuous improvement of operational efficiency and quality of service.- Direct involvement in the organization of administrative routines related to study data and files, experience with the most diverse data entry platforms used.- Excellent results with the structuring of the Clinical Trials department, implementation of control and service flows📧 slenzi.pesquisa@gmail.com