AD/Director Medical Writing

AD/Director, Medical WritingA clinical stage biotech company is seeking a senior Medical Writer to support key regulatory submissions and oncology clinical programs. This is a hands-on role for an experienced writer who is comfortable managing end to end document development and cross functional coordination, with the potential to grow into the Head of Medical Writing.Responsibilities:Lead writing and preparation of FDA submission components, clinical protocols, study reports, and related documentsCoordinate timelines, reviews, and content across Clinical, Regulatory, and BiostatsEnsure high quality, compliant documentation throughout developmentProvide hands on writing support while helping shape the medical writing functionOpportunity to grow into a future department leadership roleQualifications:8 or more years of medical writing experience in pharma or biotechStrong background in FDA submissions and clinical regulatory documentationOncology experience requiredHighly organized, detail oriented, and willing to handle both strategic and tactical work