Clinical Project Management Director
Masutoshi Toya is responsible for project managing the HBI-8000 clinical trials in Japan and subsequent regulatory activity. He is responsible for ensuring that all project timeline and milestones are met for these important registration studies. Mr. Toya has more than 20 years of drug development experience. He has worked for several pharmaceutical companies including Nippon Glaxo, Seikagaku Kogyo, Santen Pharmaceuticals and Astra Zeneca. He has both local Japanese and International clinical trials experience and has worked in a number of therapeutic areas including migraine and oncology. Mr. Toya has marketing support experience including publication planning. He received his BSc. in Pharmacy from Tokyo University of Pharmacy and Life Sciences.