[innovative Medicine] R&d, Director, Japan Medical Writing, Regulatory Medical Writing, Global Development

Johnson & Johnson

Chiyoda, Tokyo, Japan
Regulatory medical writing strategy
Japan and china medical writing
Cross-functional leadership
The Director of Regulatory Medical Writing is accountable for the strategic and operational leadership of Reg MW activities for Japan and China

Job Summary

  • The Director of Regulatory Medical Writing is accountable for the strategic and operational leadership of Reg MW activities for Japan and China.
  • This role requires strong partnership and close collaboration with senior functional and matrix leaders across Innovative Medicine R&D (IMRD) organization in Japan and China.
  • Responsible for creating an environment where employees feel engaged and empowered, and take pride in their role, responsibilities, and deliverables.

Matching Summary

The Director of Regulatory Medical Writing is accountable for the strategic and operational leadership of Reg MW activities for Japan and China.

Skills & Requirements

Must-have

  • Regulatory Medical Writing strategy
  • Japan and China medical writing
  • cross-functional leadership
  • process improvement and best practices
  • talent development and retention

Nice-to-have

  • inclusive work environment
  • proactive risk identification
  • strategic thinking and agility
  • motivating and developing talent
  • positive Credo-based work environment

Key Requirements

  • University/college degree in scientific discipline
  • 14+ years pharmaceutical/scientific experience
  • 12+ years clinical/medical writing experience
  • 5+ years people management experience
  • Expertise in project management and process improvement
  • Business Proficiency in English

Work Rights

Not specified

Tailored Resume

Cover Letter