Associate Director, Regulatory Medical Writing, Oncology

Johnson & Johnson

High Wycombe, Buckinghamshire, United Kingdom
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Regulatory medical writing
Oncology therapeutic area
Lead complex documents
** Johnson & Johnson is seeking an Associate Director for Regulatory Medical Writing specializing in Oncology to lead and oversee the writing process for clinical and regulatory documents. The ideal candidate will have extensive experience in medical writing, project management, and people management, along with a commitment to innovation in healthcare. **

Job Summary

  • Lead in setting functional tactics and strategy, and represent the therapeutic area head at high-level meetings.
  • Responsible for writing and coordinating complex clinical and regulatory documents, establishing and driving document timelines and strategies independently.
  • Supervise and manage direct reports, setting objectives, providing performance oversight, and ensuring adherence to established policies.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking an Associate Director for Regulatory Medical Writing specializing in Oncology to lead and oversee the writing process for clinical and regulatory documents. The ideal candidate will have extensive experience in medical writing, project management, and people management, along with a commitment to innovation in healthcare. **

Skills & Requirements

Must-have

  • Regulatory Medical Writing
  • Oncology therapeutic area
  • Lead complex documents
  • People management experience
  • Process improvement leadership

Nice-to-have

  • Champion internal standards
  • Develop best practices
  • Act as change agent
  • Inclusive leadership
  • Internalize CREDO behaviors

Key Requirements

  • Bachelor's Degree required
  • 10+ years pharmaceutical/scientific experience
  • 8+ years clinical/regulatory medical writing experience
  • 2+ years people management experience
  • Advanced knowledge of ICH guidelines

Work Rights

Not specified

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