Author clinical study reports (CSRs), protocols, informed consent forms (ICFs), narratives, investigator brochures, and other regulatory documents across therapeutic areas
Represent Medical Writing at meetings, drive document development, and articulate strategy and timelines
Identify the right parties for content decisions and synthesise 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

Bachelor's degree required; advanced degree preferred
Minimum 3 years of medical writing experience, including working knowledge of biostatistics
Strong knowledge of the clinical research process and applicable regulations, including ICH GCP
Clinical document reading, writing, and editing experience
Strong knowledge of MS Word, Adobe Acrobat, PowerPoint, and electronic document management systems
Ability to manage multiple projects with strong organisational, interpersonal, and communication skills

Senior Medical Writer

Key skills