Director, Medical Writing

Johnson & Johnson

Beerse, Belgium
On-site
Regulatory medical writing expertise
Cross-functional team leadership
Strategic document planning
Johnson & Johnson is seeking a Director of Medical Writing to lead strategic initiatives within their medical affairs group, ensuring high-quality document preparation across various therapeutic areas. The ideal candidate will have extensive experience in medical writing, project management, and regulatory compliance, contributing to innovative healthcare solutions

Job Summary

  • The Director of Regulatory Medical Writing is a leader with extensive medical writing expertise, serving as a primary liaison with cross-functional teams to drive strategic discussions and ensure adherence to best practices and regulatory guidelines.
  • This role involves overseeing projects, identifying risks, implementing process improvements, and guiding lead medical writers on compounds, contributing to TA-level strategies and organizational initiatives.
  • Responsibilities include acting as the primary interface for submission preparation, bringing scientific and regulatory submissions expertise, and holding cross-functional teams accountable for clinical content and MW deliverables.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Director of Medical Writing to lead strategic initiatives within their medical affairs group, ensuring high-quality document preparation across various therapeutic areas. The ideal candidate will have extensive experience in medical writing, project management, and regulatory compliance, contributing to innovative healthcare solutions.

Skills & Requirements

Must-have

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

Nice-to-have

  • Inclusive work environment
  • Commitment to innovation
  • Patient-centric approach

Key Requirements

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

Work Rights

Not specified

Tailored Resume

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