Remote Principal Medical Writer — Regulatory Dossier Expert

A leading pharmaceutical company is seeking a Principal Medical Writer to write and oversee the completion of clinical regulatory documents. This remote role requires at least 4 years of writing experience in the pharmaceutical industry, collaboration with project teams, and a strong understanding of ICH guidelines. You'll ensure compliance and clarity in communication while managing multiple projects. Join a dynamic team dedicated to high-quality documentation and international standards. #J-18808-Ljbffr