[innovative Medicine] Project Lead, Regulatory Medical Writing, Japan Document Management Group, Ib Translation Office/publication Owner Office

Johnson & Johnson

Chiyoda, Tokyo, Japan
Not specified
Drug development understanding
Project management skills
Cross-functional team experience
Johnson & Johnson is seeking a Project Lead for Regulatory Medical Writing within its Japan Document Management Group. The role focuses on managing projects related to translation and publication, with an emphasis on leveraging innovative technology like AI to enhance efficiency

Job Summary

  • Manage the daily progress of projects for translation office (Protocol, IB) and Publication Owner.
  • Own the transformation of the IB translation process from the traditional outsourcing model to an efficient process that applies the latest technology, such as AI translation.
  • Strengthen team members and lead them to cultivate their development.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Project Lead for Regulatory Medical Writing within its Japan Document Management Group. The role focuses on managing projects related to translation and publication, with an emphasis on leveraging innovative technology like AI to enhance efficiency.

Skills & Requirements

Must-have

  • drug development understanding
  • project management skills
  • cross-functional team experience
  • leading large projects
  • AI translation process transformation
  • Japanese speaking/writing skills

Nice-to-have

  • groundbreaking technologies passion
  • building processes from new viewpoint
  • influencing those around them
  • clinical trial result publication experience
  • sophisticated IT skills

Key Requirements

  • MS or advanced degree with 8+ years experience
  • BS with 10+ years experience
  • PMP certification highly desirable
  • Proficient business English conversation skills

Work Rights

Not specified

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