BACKGROUND
FOCUS AREAS
More than 20 years of global leadership experience in clinical development in a big pharma.
7 years of drug discovery research experience as a research scientist in a big pharma.
Clinical development
Regulatory strategies
As a principal consultant of ELIQUENT Japan, Takeo provides strategic and scientific initiatives for the product development of clients, managing cross-functional teams, communicating with the regulatory authorities in Japan, and driving establishment of comprehensive product development strategy.
By building effective relationships with clients and external stakeholders, Takeo contributes to the achievement of the goal of the project, also being responsible for financial, operational and timeline management.
With more than 20 years of global leadership experience in clinical development, expertise across a wide range of disease areas such as hematology, urology, and endocrinology, and experience in drug development across diverse modalities from small molecules to cell therapies, Takeo provides clients with comprehensive support for drug development from all perspectives, including development strategies and regulatory strategies.
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Education:
Ph.D., The University of Tokyo
M.S., The University of Tokyo
B.S., The University of Tokyo -
Professional experience:
Clinical development – Yamanouchi Pharmaceutical Co., Ltd./Astellas Pharma Inc.
Drug discovery research – Yamanouchi Pharmaceutical Co., Ltd.Leadership positions:
Global project leaderAreas of expertise:
Formulation of clinical development and regulatory strategies
Organic chemistry for drug discovery research
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