Vladimir (Vlado) Misik is Vice President of Global Clinical Trial Strategy at Sesen, where he leads initiatives in clinical trial localization and regulatory submission excellence. With more than 30 years of experience in biomedical R&D, regulatory strategy, and clinical operations, Vlado has helped global sponsors and CROs navigate multilingual trial execution across complex international markets. A former research scientist at The George Washington University and the NIH, he has held leadership roles at IQVIA, SanaClis, LongTaal, and VIARES. Vlado has authored over 60 publications on global clinical trials and actively contributes to DIA Core Committees and editorial boards focused on regulatory science. His insights are shaped by deep expertise in clinical trial informatics, biopharma innovation, and international regulatory frameworks.