Senior Medical Writer - Regulatory & Clinical Dossier Lead

A global biopharmaceutical company in Cambridge is looking for an experienced Senior Medical Writer to lead the preparation of high-quality clinical documentation. The candidate should have at least 5 years of Medical Writing experience in a pharmaceutical setting and a strong understanding of regulatory requirements. This role involves managing timelines for multiple projects, mentoring junior writers, and ensuring compliance with documentation standards. Join a passionate team focused on making a meaningful impact in patient care.