About this role
Senior Manager, Medical Writing at Travere. Location: San Diego or United States. Role: authoring documents, managing timelines, summarizing data Requirements: 7+ years medical/regulatory writing experience in biotech/pharma/CRO; Bachelor's in life/medical/technical sciences required (advanced degree preferred); expert scientific writing; knowledge of FDA/EMA/ICH; Microsoft Office and Veeva proficiency. Category: Research and Development (R&D) Seniority: Senior Level Tools: Microsoft Office, Veeva platforms, electronic document management systems Commitment: Full Time Workplace: Hybrid Languages: English