[innovative Medicine] R&d, Director, Japan Medical Writing, Regulatory Medical Writing, Global Development
Johnson & Johnson
Chiyoda, Tokyo, Japan
Regulatory medical writing expertise
Strategic and operational leadership
Cross-functional team 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.
The Director will influence strategies, lead process working groups, champion internal standards, and improve internal systems and tools.
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 expertise
strategic and operational leadership
cross-functional team leadership
process improvement and best practices
risk identification and mitigation
Nice-to-have
inclusive work environment
diversity and dignity of employees
positive Credo-based work environment
openness to new ideas
fosters organizational learning
Key Requirements
University/college degree in a scientific discipline
At least 14 years of relevant pharmaceutical/scientific experience
At least 12 years of relevant clinical/medical writing experience
At least 5 years of people management experience
Expertise in project management and process improvement