Director, Medical Writing

Johnson & Johnson

Allschwil, Switzerland
Base: $164,000.00 - $282,900.00; bonus/equity: eli...
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Medical writing expertise
Cross-functional team leadership
Regulatory guidelines adherence
** Johnson & Johnson is seeking a Director of Medical Writing, a leadership role that requires extensive experience in medical writing and regulatory affairs. The position involves overseeing projects, guiding teams, and driving process improvements in a collaborative environment, with the potential for remote work on a case-by-case basis. **

Job Summary

  • The Director of Regulatory Medical Writing (RegMW) is recognized as a leader with extensive medical writing expertise for documents across various therapeutic areas (TAs).
  • This role is a primary liaison with cross-functional teams, driving strategic discussions, and ensuring adherence to best practices and regulatory guidelines.
  • The Director will influence TA-level strategies, lead process working groups, champion internal standards, and improve internal systems and tools.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Director of Medical Writing, a leadership role that requires extensive experience in medical writing and regulatory affairs. The position involves overseeing projects, guiding teams, and driving process improvements in a collaborative environment, with the potential for remote work on a case-by-case basis. **

Salary

Base: $164,000.00 - $282,900.00; Bonus/Equity: Eligible for annual performance bonus; Benefits: Medical, dental, vision, life insurance, disability, retirement plan, 401(k), long-term incentive program, paid time off

Skills & Requirements

Must-have

  • Medical writing expertise
  • Cross-functional team leadership
  • Regulatory guidelines adherence
  • Strategic submission planning
  • Process improvement implementation

Nice-to-have

  • Patient-centric approach
  • Inclusive work environment
  • Mentoring and coaching staff
  • Industry standards representation

Key Requirements

  • 14+ years pharmaceutical/scientific experience
  • 12+ years clinical/medical writing experience
  • Expertise in project management
  • Expertise in process improvement
  • University/college degree in scientific discipline

Work Rights

Not specified

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