Director Medical Writing Asset Lead

GSK

Base: pln 0 to pln 0 gross; bonus/equity: eligible...
Clinical regulatory writing experience
Ich/gcp and global regulatory guidelines
Strategic and critical thinking
As Medical Writing Asset Lead Director, you will apply experience, scientific and operational expertise, and leadership in a matrix organization to provide the medical writing strategy for one or more assets

Job Summary

  • As Medical Writing Asset Lead Director, you will apply experience, scientific and operational expertise, and leadership in a matrix organization to provide the medical writing strategy for one or more assets.
  • You will balance scientific rigor with practical execution, champion efficient and accelerated ways of working, and proactively identify opportunities to simplify document lifecycle, reduce risk and strengthen submission quality across the asset lifecycle.
  • This role offers meaningful impact, visible growth opportunities, and a chance to unite science, technology and talent to get ahead of disease together.

Matching Summary

As Medical Writing Asset Lead Director, you will apply experience, scientific and operational expertise, and leadership in a matrix organization to provide the medical writing strategy for one or more assets.

Salary

Base: PLN 0 to PLN 0 gross; Bonus/Equity: eligible for a bonus (if applicable); Benefits: statutory benefits, private healthcare, additional paid days off, life insurance, private pension plan, fully paid parental leave & care of family member leave

Skills & Requirements

Must-have

  • clinical regulatory writing experience
  • ICH/GCP and global regulatory guidelines
  • strategic and critical thinking
  • leading matrix teams
  • clinical document strategy

Nice-to-have

  • collaborative leaders
  • practical problem solving
  • inclusive coaching
  • agile working culture
  • accelerated submissions experience

Key Requirements

  • Postgraduate degree in life sciences, pharmacy, medicine, public health or related discipline
  • Extensive experience in clinical regulatory writing
  • Extensive experience in project management
  • Excellent understanding of clinical operations / medical writing processes
  • Strong problem solving, influencing and decision-making capabilities

Work Rights

Not specified

Tailored Resume

Cover Letter