# Senior Director, Global Regulatory Affairs, Neurology at Eisai Us

- Company: Eisai Us
- What the company does: Eisai Inc. (pronounced ā-zī) is a U.S. pharmaceutical subsidiary of Tokyo-based Eisai Co., Ltd., a research-based human health care (HHC) company that discovers, develops, and markets products throughout the world. Established in 1995, Eisai Inc. Backed by North Carolina Biotechnology Center.
- Company website: https://us.eisai.com
- Type: Startups
- Level: Principal and up
- Location: 2 Locations
- Work setup: On-site
- Pay: $249K to $327K base salary per year (USD)
- Posted: 2026-09-23
- Apply by: 2026-11-07
- Apply: https://eisai.wd5.myworkdayjobs.com/en-US/eisai/job/New-Jersey-Nutley/Senior-Director--Global-Regulatory-Affairs--Neurology_R4214
- Page: https://www.1752.vc/careers/jobs/eisai-us-senior-director-global-regulatory-affairs-neurology/

## About the role

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission. We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer’s disease.

## What they're looking for

- Bachelor's degree (Master's preferred) and 12+ years of relevant experience
- Bachelor's or advanced degree in sciences or related field with significant experience in regulatory/R&D area with drug development and regulatory experience in pharma/biotech industry
- OR a combination of equivalent education and experience
- Proven experience in strategy development within area, operational management of regulatory strategy processes through cross-functional teams, as well as budget planning & management
- Demonstrated experience/working knowledge in the design and process of clinical trials including clinical data collection and analysis and preparation of regulatory submissions, preferred
- Demonstrated track record of interfacing effectively with FDA with some experience with health authorities, extensive experience with FDA laws, regulations and guidances, as well international regulation