Senior Medical Writer Regulatory Submissions Lead

MMS, a data-focused CRO, seeks an experienced Medical Writer in New York to critically evaluate literature, select materials for study design, and prepare regulatory documents. You will write and edit protocols, investigators' brochures, study reports, consent forms, safety summaries, and modules to regulatory standards. You will mentor team members, coordinate with clients to ensure timely delivery, and maintain high quality across multiple documents while adhering to strict timelines.