Senior Medical Writer — Regulatory & Protocol Expert

A leading clinical research organization is seeking a full-time Medical Writer to work remotely in the UK. In this role, you will evaluate medical literature, write clinical development documents, and manage various writing assignments. The ideal candidate will possess a Bachelor’s, Master’s, or PhD in a relevant field, along with at least 6 years of regulatory writing experience. Exceptional writing skills and the ability to lead projects under aggressive timelines are essential for success in this role. #J-18808-Ljbffr