Senior Medical Writer

GlaxoSmithKline

Poland
Base: pln 166,500 to pln 277,500 gross; bonus/equi...
Not specified in the job posting.
Clinical trial design understanding
Interpretation of clinical research data
Drafting regulatory documents
GlaxoSmithKline (GSK) is seeking a Senior Medical Writer in Poland, responsible for creating and reviewing complex clinical documents while coordinating with various stakeholders. The ideal candidate will possess strong regulatory writing experience, a solid understanding of clinical data interpretation, and excellent communication skills

Job Summary

  • The Senior Medical Writer is expected to work on assignments largely independently or for complex documents, under guidance of a mentor, facilitating delivery of the written assignments through proactive coordination of stakeholders to build content.
  • Authors a range of clinical documents, including regulatory documents following defined templates, including but not limited to protocols, clinical study reports, NDA/MAA CTD submission documents, investigator brochures, briefing documents, and responses to regulatory authority questions.
  • You will join a team that values respectful collaboration, continuous learning and accountability.

Matching Summary

Match Score: 85

GlaxoSmithKline (GSK) is seeking a Senior Medical Writer in Poland, responsible for creating and reviewing complex clinical documents while coordinating with various stakeholders. The ideal candidate will possess strong regulatory writing experience, a solid understanding of clinical data interpretation, and excellent communication skills.

Salary

Base: PLN 166,500 to PLN 277,500 gross; Bonus/Equity: potentially eligible for bonus; 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 trial design understanding
  • interpretation of clinical research data
  • drafting regulatory documents
  • ICH/GCP knowledge
  • proactive stakeholder coordination

Nice-to-have

  • ambitious for patients culture
  • accountable for impact mindset
  • continuous learning environment
  • respectful collaboration

Key Requirements

  • Up to 5 years clinical regulatory writing experience
  • Basic drug development understanding
  • Scientific methodology and statistical principles knowledge
  • Ability to work on 2-3 assignments simultaneously

Work Rights

Not specified

Tailored Resume

Cover Letter