[innovative Medicine] R&d, Director, Japan Medical Writing, Regulatory Medical Writing, Global Development
Johnson & Johnson
Chiyoda, Tokyo, Japan
Regulatory medical writing expertise
Cross-functional team leadership
Process improvement and project management
The Director of Regulatory Medical Writing is accountable for strategic and operational leadership of medical writing activities for Japan and China, driving high-quality and compliant portfolio delivery
Job Summary
The Director of Regulatory Medical Writing is accountable for strategic and operational leadership of medical writing activities for Japan and China, driving high-quality and compliant portfolio delivery.
This role involves mentoring staff, leading process improvements, and collaborating closely with senior leaders across Innovative Medicine R&D to ensure alignment with regulatory guidelines and organizational goals.
Johnson & Johnson fosters an inclusive work environment that respects diversity and empowers employees to take pride in their roles and deliverables.
Matching Summary
The Director of Regulatory Medical Writing is accountable for strategic and operational leadership of medical writing activities for Japan and China, driving high-quality and compliant portfolio delivery.
Skills & Requirements
Must-have
Regulatory medical writing expertise
Cross-functional team leadership
Process improvement and project management
Strategic decision-making authority
Medical writing team development
Collaboration with global R&D organizations
Nice-to-have
Inclusive leadership
Mentoring and coaching skills
Positive Credo-based work environment
Organizational learning and openness
Talent pipeline development
Key Requirements
University degree in scientific discipline
Advanced degree preferred (Masters, PhD, MD)
At least 14 years pharmaceutical/scientific experience
Minimum 12 years clinical/medical writing experience