About this role
Regulatory Writer and/or Regulatory QC/ Editor at Vir Biotechnology. Location: United States. Role: writing documents, reviewing documents, managing workflows Requirements: Bachelor's degree and 5+ years relevant experience; working knowledge of eCTD/CTD documents, ICH/FDA/EMA guidance; experience with Veeva Vault and SmartSheet; strong attention to detail and critical thinking. Category: Research and Development (R&D) Seniority: Senior Level Tools: Veeva Vault, SmartSheet, eCTD/CTD, AMA Manual of Style Commitment: Contract, Temporary Workplace: Remote Languages: English