Director Medical Writing Asset Lead

GSK

Base: pln 0 to pln 0 gross in pol + ; bonus/equity...
Not specified
Clinical regulatory writing expertise
Matrix leadership and project management
Knowledge of ich/gcp and global regulatory guidelines
GSK is seeking a Director Medical Writing Asset Lead to provide medical writing strategy for clinical documents related to regulatory submissions. The ideal candidate will have extensive experience in clinical regulatory writing, project management, and leadership in a matrix organization, fostering a culture of accountability and ambition for patient outcomes

Job Summary

  • As Medical Writing Asset Lead Director, you will design and deliver high-quality clinical documents for global regulatory submissions while leading matrix teams and collaborating with multiple stakeholders.
  • The role offers meaningful impact, visible growth opportunities, and a chance to unite science, technology, and talent to advance disease treatment.
  • GSK provides a comprehensive benefits package including private healthcare, paid leave, life insurance, and a culture committed to patient impact and inclusive leadership.

Matching Summary

Match Score: 85

GSK is seeking a Director Medical Writing Asset Lead to provide medical writing strategy for clinical documents related to regulatory submissions. The ideal candidate will have extensive experience in clinical regulatory writing, project management, and leadership in a matrix organization, fostering a culture of accountability and ambition for patient outcomes.

Salary

Base: PLN 0 to PLN 0 gross in Poland; Bonus/Equity: Eligible for bonus and awards based on performance; Benefits: Private healthcare, paid leave, life insurance, pension plan, 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
  • collaboration 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 mindset
  • strong strategic and critical thinking skills

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter