Associate Director, X-ta Regulatory Medical Writing

Johnson & Johnson

High Wycombe, Buckinghamshire, United Kingdom
Base: $137,000 to $235,750 usd (us only); bonus: a...
3d onsite
10 years pharmaceutical experience
8 years medical writing experience
2 years people management experience
This role involves leading compound and submission writing teams independently while managing direct reports in a hybrid work environment

Job Summary

  • This role involves leading compound and submission writing teams independently while managing direct reports in a hybrid work environment.
  • The position requires preparing and finalizing all types of clinical documents with a proactive role in scientific strategy and regulatory guidelines.
  • Candidates will benefit from competitive performance-based compensation, annual bonuses, and comprehensive benefits including medical, dental, vision, and retirement plans.

Matching Summary

This role involves leading compound and submission writing teams independently while managing direct reports in a hybrid work environment.

Salary

Base: $137,000 to $235,750 USD (US only); Bonus: Annual performance bonus eligible; Benefits: Medical, dental, vision, life insurance, 401(k), vacation up to 120 hours

Skills & Requirements

Must-have

  • 10 years pharmaceutical experience
  • 8 years medical writing experience
  • 2 years people management experience
  • Scientific discipline degree required
  • Lead clinical document preparation

Nice-to-have

  • Multiple therapeutic area experience
  • Cross-functional collaboration skills
  • Process improvement leadership
  • Masters or PhD preferred
  • Inclusive leadership approach

Key Requirements

  • University degree in scientific discipline
  • Minimum 10 years relevant pharma experience
  • Minimum 8 years medical writing experience
  • Minimum 2 years people management experience
  • Fluent written and spoken English

Work Rights

Not specified

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