Medical Writing Expert

2 dni temu


Poznań, Greater Poland GlaxoSmithKline Pełny etat

Job Description:

GSK seeks a talented and experienced Senior Medical Writer to join our team. As a key member of our medical writing department, you will be responsible for creating high-quality clinical documents, including regulatory documents, protocols, and clinical study reports.

About the Role:

  • You will work on assignments independently or under the guidance of a mentor to deliver written content that meets the company's quality standards.
  • Your expertise in clinical trials design, data interpretation, and statistical principles will enable you to create accurate and compelling content.
  • You will collaborate with cross-functional teams, including clinical leads, asset leads, and biostatisticians, to ensure seamless delivery of writing assignments.
  • Your strong communication skills and ability to build partnerships will facilitate smooth interfaces between teams.

Requirements:

  • A PhD or equivalent expertise, or a master's degree with a minimum of 2 years' relevant experience.
  • Up to 5 years of clinical regulatory writing experience in the pharmaceutical industry.
  • A good understanding of basic drug development and scientific methodology.
  • Knowledge of International Committee for Harmonisation (ICH) / Good Clinical Practice (GCP).
  • Excellent English language skills (verbal and written).

Benefits:

  • Career opportunities at a leading global healthcare company.
  • An attractive reward package, including annual bonus, awards for outstanding performance, recognition awards, holiday benefit, and life insurance.
  • Hybrid working model with flexible working solutions.
  • Extensive support for work-life balance, including health and well-being activities.


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