Senior Medical Writer

Author clinical study reports, protocols, informed consent forms, narratives, and investigator brochures while collaborating with clinical teams and biostatisticians. Represent Medical Writing at meetings, drive document development, and articulate strategy and timelines. Identify the right parties for content decisions and synthesize discussions into clear, accurate prose. Review work of junior or outsourced writers and CSR-related documents like Statistical Analysis Plans and TFLs. Write plain-language content such as ICFs and explain complex medical concepts to lay audiences. Adhere to applicable guidelines, templates, SOPs, and internal training while contributing to process improvement across Medical Writing and Global Development. Mentor junior staff, manage multiple priorities, and foster collaboration to resolve conflict.