About this role
Principal Medical Writer at Gsk. Location: Durham or London. Role: authoring documents, managing projects, translating data Requirements: Bachelor's in life/health/scientific field, 5+ years medical or regulatory writing in pharma, 3+ years regulatory dossier and CTD experience, 3+ years independently authoring protocols and clinical study reports; strong writing, teamwork, and regulatory knowledge. Category: Research and Development (R&D) Seniority: Senior Level Tools: Common Technical Document (CTD), International Council for Harmonisation (ICH), Good Clinical Practice (GCP) Commitment: Full Time Workplace: Onsite Languages: English