About the role

Daiichi Sankyo US in New Jersey seeks a Global Regulatory Lead to shape regulatory strategy for development programs and represent regulatory in GPT meetings. You will guide submissions, align regional plans, and ensure Health Authority alignment across global programs.
Required: 7+ years in regulatory affairs with NDA/BLA experience including the US, and strong cross‑functional leadership in oncology-focused development. Travel up to 20%.

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JOB OVERVIEW

Experience level

Manager

Location

Basking Ridge, NJ

Occupation

Regulatory Affairs Managers

Industry

Research and Development in Biotechnology (except Nanobiotechnology)

Posted

yesterday

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