Director, Medical Writing

Johnson & Johnson

Allschwil, Switzerland
$164,000.00 - $282,900.00; bonus/equity: eligible ...
On-site
Regulatory medical writing expertise
Cross-functional team leadership
Strategic submission planning
Johnson & Johnson is seeking a Director of Medical Writing with extensive experience in regulatory and clinical writing across various therapeutic areas. The role requires strong leadership capabilities and strategic thinking to oversee projects, collaborate with cross-functional teams, and mentor junior writers

Job Summary

  • Assume overall accountability for decision-making within the organization or TA, ensuring alignment with strategic goals.
  • Provide guidance to other writers on all types of clinical, regulatory, and safety documents, taking a proactive lead in content and scientific strategy with complete independence.
  • Act as the primary interface with the Compound Development Teams (CDTs) at the early stages of submission preparation and as a MW expert for the delivery of Johnson & Johnson Innovative Medicine marketing applications.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Director of Medical Writing with extensive experience in regulatory and clinical writing across various therapeutic areas. The role requires strong leadership capabilities and strategic thinking to oversee projects, collaborate with cross-functional teams, and mentor junior writers.

Salary

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

Skills & Requirements

Must-have

  • Regulatory Medical Writing expertise
  • Cross-functional team leadership
  • Strategic submission planning
  • Process improvement implementation
  • Mentoring and coaching staff

Nice-to-have

  • Innovative Medicine development
  • Patient-centric approach
  • Credo-based work environment
  • Openness to new ideas

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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