Senior Medical Writer

GlaxoSmithKline

Poland
Base: pln 166,500 to pln 277,500 gross; bonus/equi...
On-site
Clinical trial design interpretation
Statistically analysed clinical research data
Draft, review, and approve written assignments
GlaxoSmithKline is seeking a Senior Medical Writer in Poland, responsible for drafting and coordinating clinical regulatory documents. The ideal candidate will possess up to five years of relevant writing experience in the pharmaceutical industry, with a strong understanding of clinical trial data and regulatory requirements

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 is seeking a Senior Medical Writer in Poland, responsible for drafting and coordinating clinical regulatory documents. The ideal candidate will possess up to five years of relevant writing experience in the pharmaceutical industry, with a strong understanding of clinical trial data and regulatory requirements.

Salary

Base: PLN 166,500 to PLN 277,500 gross; Bonus/Equity: Eligible for bonus and/or awards for exceptional performance; 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 interpretation
  • statistically analysed clinical research data
  • draft, review, and approve written assignments
  • high integrity of data interpretation
  • consistency and quality of documents
  • proactive communication with stakeholders

Nice-to-have

  • ambitious for patients
  • accountable for impact
  • committed to doing the right thing
  • respectful collaboration
  • continuous learning

Key Requirements

  • Up to 5 years clinical regulatory writing experience
  • Good understanding of basic drug development
  • Knowledge of scientific methodology and statistical principles
  • Understanding of how to interpret, describe and document clinical data
  • Working knowledge of ICH/GCP

Work Rights

Not specified

Tailored Resume

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