Principal Medical Writer
RemoteUnited Kingdom or United States
United Kingdom or United StatesRemoteFull TimeSenior LevelBIOTECHSmall
Full TimeSenior LevelSmallBIOTECH
Job Summary
Organize, analyze, interpret, and present scientific and statistical information in accordance with ICH guidelines and company document standards while independently planning and preparing regulatory documents and medical communications across all product development phases. Collaborate with cross-functional internal and external document production teams under the direction of Medical Writing management. This role supports Veristat's global team of 105+ approved therapies and 480+ oncology projects, offering flexible remote work options and a 70% remote workforce culture.
Required Qualifications
- Bachelor's degree
- science-related field
- Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting
- Advanced knowledge of ICH and related regulatory guidelines
- Excellent written English
- keen attention to detail
- Strong interpersonal and communication skills
- Experience with Microsoft Office Suite
- advanced Microsoft Word proficiency
Desired Qualifications
- science-related field preferred
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