Sara Acedo

Sara Acedo has over 20 years of diverse experience in clinical trials and accounting. Currently serving as a Global Clinical Supplies Label Coordinator at PPD since November 2013, Sara effectively plans and executes label and patient card activities for clinical studies. Prior experience at PPD includes roles as a Subject Matter Expert and Principal Clinical Trial Coordinator, where responsibilities included providing feedback to approximately 40 Project Assistants and supporting quality and risk management. Previous positions at Merck and Johnson & Johnson furthered expertise in managing trial documentation and accounting processes. Sara's educational background includes a Clinical Trial Assistant Course from Fundación ESAME and an Administration and Finance Superior Technician diploma from I.E.S. Manuel de Falla.