Associate Director, Regulatory Medical Writing, Oncology

Johnson & Johnson Innovative Medicine

Allschwil, Switzerland
$137,000 to $235,750; bonus: annual performance bo...
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Lead regulatory medical writing
Oncology therapeutic area
Clinical and regulatory documents
** Johnson & Johnson is seeking an Associate Director of Regulatory Medical Writing in Oncology, responsible for leading medical writing efforts and ensuring compliance with regulatory standards. The role requires extensive experience in pharmaceutical writing, project management, and team leadership while offering a fully remote work option. **

Job Summary

  • Lead compound/submission/indication/disease area writing teams independently, taking a proactive or lead role in terms of content and scientific strategy.
  • Contribute to and champion internal standards, regulatory, and publishing guidelines, as well as the improvement of internal systems, tools, and processes.
  • This position is eligible for an annual performance bonus, and employees are eligible for comprehensive benefits including medical, dental, vision, retirement plans, and various time off benefits.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking an Associate Director of Regulatory Medical Writing in Oncology, responsible for leading medical writing efforts and ensuring compliance with regulatory standards. The role requires extensive experience in pharmaceutical writing, project management, and team leadership while offering a fully remote work option. **

Salary

$137,000 to $235,750; Bonus: Annual performance bonus; Benefits: Medical, dental, vision, life insurance, disability, retirement, time off

Skills & Requirements

Must-have

  • Lead regulatory medical writing
  • Oncology therapeutic area
  • Clinical and regulatory documents
  • ICH guidelines
  • People management experience

Nice-to-have

  • Cross-functional collaboration
  • Process improvement initiatives
  • Mentoring junior writers
  • Acting as change agent

Key Requirements

  • Bachelor's Degree required
  • 10 years pharmaceutical/scientific experience
  • 8 years clinical/regulatory medical writing
  • 2 years people management experience

Work Rights

Not specified

Tailored Resume

Cover Letter