Director, Medical Writing

Johnson & Johnson

Beerse, Belgium
On-site
Medical writing expertise
Regulatory guidelines adherence
Cross-functional team leadership
Johnson & Johnson is seeking a Director of Medical Writing to lead strategic discussions and oversee projects in the field of medical writing, particularly within the Innovative Medicine sector. This role requires extensive experience in clinical and regulatory writing, as well as strong leadership and project management skills

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 and ensuring adherence to best practices and regulatory guidelines.
  • This role involves overseeing projects, identifying risks, implementing process improvements, and guiding lead medical writers on compounds, while influencing TA-level strategies and championing internal standards.
  • The Director will act as the primary interface for submission preparation, bringing scientific and regulatory expertise to marketing applications and holding cross-functional teams accountable for clinical content delivery.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Director of Medical Writing to lead strategic discussions and oversee projects in the field of medical writing, particularly within the Innovative Medicine sector. This role requires extensive experience in clinical and regulatory writing, as well as strong leadership and project management skills.

Skills & Requirements

Must-have

  • medical writing expertise
  • regulatory guidelines adherence
  • cross-functional team leadership
  • strategic submission planning
  • process improvement implementation

Nice-to-have

  • inclusive work environment
  • championing patients
  • mentoring and coaching staff
  • knowledge of industry guidelines
  • positive Credo-based work environment

Key Requirements

  • University/college degree in 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

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