Thuy Vo

Thuy Vo has extensive experience in clinical trial management, having served in multiple roles across various organizations. Starting as a Clinical Trial Assistant at Cmed Clinical Services and later at IQVIA, Thuy developed foundational skills in handling clinical documentation, managing study trackers, and ensuring compliance with regulatory standards. Progressing to positions at ExecuPharm and Seagen as a Senior Clinical Trials Associate, Thuy gained expertise in investigational product supply, resolution of supply issues, and regulatory packet collection for site start-up. Currently, Thuy is a Clinical Study Team Assistant at Pfizer, directing CTA tasks for CRO outsourced studies and coordinating complex trial operations. Thuy holds both a Master of Science and a Bachelor of Science in Clinical Research from Campbell University.