
This senior leadership role at Daiichi Sankyo involves directing regulatory strategy for U.S. advertising and promotion across the company's pharmaceutical portfolio. The Director serves as a subject matter expert, leading the review of complex promotional materials to ensure strict compliance with FDA regulations and approved labeling while balancing business objectives. Key responsibilities include providing strategic counsel to cross-functional teams on claims development and launch communications, managing interactions with health authorities, and refining internal review processes and standards. The position offers the opportunity to shape compliant messaging for breakthrough therapies in oncology and other therapeutic areas within a global, mission-driven organization. The role is based in an in-house office with occasional travel requirements.


















