Director Medical Writing Asset Lead

Gsicareers

Unknown
Base: pln 0 to pln 0 gross in pol + ; bonus/equity...
Clinical regulatory writing expertise
Matrix leadership and project management
Knowledge of ich/gcp and global regulatory guidelines
As Medical Writing Asset Lead Director, you will design and deliver high-quality clinical documents for global regulatory submissions and contribute to organizational process improvements

Job Summary

  • As Medical Writing Asset Lead Director, you will design and deliver high-quality clinical documents for global regulatory submissions and contribute to organizational process improvements.
  • The role offers meaningful impact, visible growth opportunities, and a chance to unite science, technology and talent to get ahead of disease together.
  • GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, ensuring a collaborative and high-performing work environment.

Matching Summary

As Medical Writing Asset Lead Director, you will design and deliver high-quality clinical documents for global regulatory submissions and contribute to organizational process improvements.

Salary

Base: PLN 0 to PLN 0 gross in Poland; Bonus/Equity: Eligible for bonus and awards based on criteria; Benefits: Private healthcare, paid days off, life insurance, pension, parental leave

Skills & Requirements

Must-have

  • clinical regulatory writing expertise
  • matrix leadership and project management
  • knowledge of ICH/GCP and global regulatory guidelines
  • planning and delivering global regulatory submissions
  • collaborating with cross-functional teams

Nice-to-have

  • experience with accelerated submissions
  • clinical pharmacology and PK/PD interpretation
  • mentoring and training capabilities
  • process improvement and simplification
  • strong strategic and critical thinking

Key Requirements

  • Postgraduate degree in life sciences or related discipline
  • Extensive experience in clinical regulatory writing
  • Proven track record in clinical document authorship
  • Extensive project management and matrix leadership experience
  • Excellent understanding of clinical operations and regulatory guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter