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Jobs / Regulatory Affairs Specialist in United States of America
21 days ago
Eisai·21 days ago
21 days ago

Senior Director, Global Regulatory Affairs, Neurology

Nutley, United States of AmericaFull-timeSenior · 10-15 yearsRegulatory Affairs Specialist

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Must-have skills for this role

  • regulatory strategy
  • regulatory submissions
  • fda compliance
  • regulatory affairs

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What you'll do

  • Lead regulatory strategy and submissions for Eisai’s Neurology and Oncology portfolio
  • Oversee regulatory activities
  • Ensure compliance
  • Drive strategic initiatives

Summarised by NextRaise from the employer’s description, which follows in full below.

Full description from employer

Join us as Senior Director, Global Regulatory Affairs, Neurology to lead regulatory strategy and submissions for Eisai’s Neurology and Oncology portfolio. Oversee regulatory activities, ensure compliance, and drive strategic initiatives. Ideal for experienced professionals with a strong background in regulatory affairs and leadership within the life sciences sector.

Skills

  • regulatory strategy
  • regulatory submissions
  • fda compliance
  • clinical trials
  • regulatory strategy development
  • project management
  • budget management
  • vendor management
  • cross-functional team leadership
  • health authority engagement
  • risk management
  • regulatory affairs
  • life sciences industry knowledge
  • regulatory strategy process improvement
  • scientific data analysis
  • regulatory strategy planning
  • stakeholder management
  • performance management
  • mentoring
  • business agility
  • critical thinking

Company

Eisai
Nutley, United States of America

Company facts come from this company's own listings. We only show what the postings themselves carry.

Sourced from Eisai·first seen 31 Aug 2026·last verified 8 Sept 2026·How we source jobs

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