Associate Director, Regulatory Medical Writing, Oncology

Johnson & Johnson UK

Beerse, Belgium
Fully remote
10 years of pharmaceutical experience
8 years of medical writing experience
2 years of people management experience
Johnson & Johnson is seeking an Associate Director of Regulatory Medical Writing in Oncology, a role focused on leading medical writing efforts for complex documents and managing a team of writers. The position emphasizes project management, regulatory compliance, and cross-functional collaboration, supporting innovative treatments and drug development

Job Summary

  • Join Johnson & Johnson in developing treatments and finding cures for cancer.
  • Lead writing teams and manage internal medical writers to ensure quality deliverables.
  • Contribute to process improvements and mentor junior writers in a collaborative environment.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking an Associate Director of Regulatory Medical Writing in Oncology, a role focused on leading medical writing efforts for complex documents and managing a team of writers. The position emphasizes project management, regulatory compliance, and cross-functional collaboration, supporting innovative treatments and drug development.

Skills & Requirements

Must-have

  • 10 years of pharmaceutical experience
  • 8 years of medical writing experience
  • 2 years of people management experience

Nice-to-have

  • Strong leadership skills
  • Expert project management skills
  • Ability to build relationships

Key Requirements

  • Bachelor's degree required
  • Advanced degree preferred

Work Rights

Not specified

Tailored Resume

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