Director Medical Writing Asset Lead

GlaxoSmithKline

Poland
Base: pln 0 to pln 0 gross; bonus/equity: bonus ma...
Clinical regulatory writing experience
Clinical document strategy
Leading matrix teams
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 design and deliver high-quality fit for purpose clinical documents for global regulatory submissions, plan for efficient and accelerated ways of working, and contribute to key organizational process improvements.
  • GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success.

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: Bonus may be eligible; 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
  • clinical document strategy
  • leading matrix teams
  • global regulatory submissions
  • ICH/GCP and global regulatory guidelines

Nice-to-have

  • collaborative leaders
  • scientific rigor
  • practical problem solving
  • inclusive coaching
  • agile working culture

Key Requirements

  • Postgraduate degree in life sciences or related discipline
  • Extensive experience in clinical regulatory writing
  • Extensive experience in project management
  • Demonstrated matrix leadership
  • Excellent understanding of clinical operations / medical writing processes

Work Rights

Not specified

Tailored Resume

Cover Letter