Biomedical Data Scientist with a strong foundation in Biomedical Sciences (Molecular Biology, Physiology) and advanced expertise in Data Science & Analytics, coupled with multifaceted experience in Clinical Trials and Regulatory Affairs. BSc in Biomedical Sciences (Universidade Cruzeiro do Sul, Dec/2020); currently pursuing a Postgraduate program in Data Science & Analytics at the University of São Paulo (USP). Over six years in the Pharmaceutical Industry and CROs, progressing from Preclinical Research/Scientific Initiation to support for Clinical Trials (Phases III/IV and Access Programs), encompassing on-site monitoring, Pharmacovigilance, Quality, and Regulatory Affairs. Specialized in multicenter studies and clinical supply management, coordinating imports, on-demand planning, and serving as the focal point for Industry-Sponsored Studies (IIS) in collaboration with key opinion leaders and internal stakeholders. Since early 2024, working as a Study Start-up Associate in Evidence Generation, actively applying Data Science in regulatory contexts and Real-World Evidence (RWE). Responsible for developing and maintaining Power BI dashboards and reports; analyzing and interpreting large datasets (real-world data, public datasets such as SUS, and real-time data) to identify strategic insights and trends for leadership. Deep knowledge of RIM (Records and Information Management) aligned to current and emerging compliance regulations, ensuring data integrity and quality across the lifecycle. Recognized for being highly organized, creative, and collaborative, with strong leadership skills and a steadfast commitment to quality, integrity, and data governance throughout research and analytics. Keywords: RWE; Real-World Data; Clinical Trials; Study Start-up; Evidence Generation; Regulatory Affairs; Records and Information Management (RIM); Data Governance; Power BI; Analytics; Multicenter Studies; Clinical Supply Management; DATASUS (Brazil).