Sofia Leal

Sofia Leal is an experienced professional in the clinical trials and regulatory affairs sectors, currently serving as an Applicatiebeheerder EPD & BIOSLIMS at UZA since March 2021. Prior experience includes roles as Regional Study Coordinator at Covance, where responsibilities involved managing clinical trial activities and collaborating with global teams, as well as serving as a Clinical Safety Associate and Regulatory Affairs Associate at genae, focusing on regulatory submissions across multiple countries. Earlier positions at LabCorp Clinical Trials featured roles in study initiation, clinical database design, and clinical trials monitoring, showcasing a comprehensive understanding of trial processes and regulatory requirements. Sofia Leal holds a degree in Graphic Design from the Universidade do Porto.