Medical Writing Expert
2 dni temu
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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