Principal Medical Writer - Regulatory Documents & Strategy

Precision Medicine Group is seeking a Senior Medical Writer/Principal Medical Writer to lead the development of clinical study documents in a fast-paced setting in the United States. You will plan, write, edit, format, and QC protocols, IBs, CSR narratives, and consent templates with meticulous attention to regulatory requirements. Responsibilities include end-to-end document management with sponsors and vendors, extracting key messages from study data, and contributing to SOPs and templates.