Taiho Oncology, Inc. seeks a senior Director to lead global regulatory CMC activities, coordinating strategy, submissions, and approvals across US, EU, and other regions. This role partners with internal teams and external consultants to ensure compliant development and post-approval activities. With extensive CMC expertise, you will influence regulatory strategies, manage interactions with authorities, and drive submission planning for NDA/MAA developments, while guiding teams across functions

Also on the board Same function, level within a rung

Level

Manager

Location

Pleasanton, CA

Occupation

Regulatory Affairs Managers

Industry

Research and Development in Biotechnology (except Nanobiotechnology)

Posted

yesterday

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