Senior Medical Writer - Regulatory Documentation & QA Lead

CTC in Basel seeks an experienced Clinical/Regulatory Quality Assurance professional to lead and optimize the quality of regulatory documents for NDA/MAA/IND submissions. You will collaborate with authors and cross-functional teams to drive excellence in documentation and templates.The role requires a Master’s degree (science-related preferred) and 10+ years in QA, medical or regulatory writing, and document quality review, with fluency in English and additional European languages as an #J-18808-Ljbffr