Director, Companion Diagnostics Regulatory Affairs

Daiichi Sankyo, Inc. is seeking a senior regulatory leader to drive global CDx/IVD regulatory strategy for oncology products.

You will guide development programs, craft submission plans, and align regulatory activities across regions to maximize patient access and data quality. Responsibilities include coordinating with regional teams, managing FDA/EMA interactions, and ensuring timely registrations of both therapeutic and diagnostic assets in major markets.