Regulatory Medical Writer — AI Documentation Review

Role overview Apply your clinical and regulatory writing expertise to improve AI-assisted documentation tools. You will judge whether draft clinical documents are accurate, well structured and supported by the underlying evidence. What you’ll be doing • Create and review realistic evaluation tasks based on Clinical Study Reports and periodic safety documents. • Assess draft content for scientific accuracy, document structure, cross-references and appropriate use of source records. • Explain errors and provide structured feedback that helps improve evaluation guidance. Who this could suit Experienced medical writers and clinical document authors who have led substantial regulatory writing projects. Prior AI training experience is not required. What you’ll need The listing prefers at least five years of regulatory medical writing experience and direct experience authoring full Clinical Study Reports. You should understand ICH E3 and relevant safety-document conventions, be able to interpret tables, figures, listings and protocols, and write clear, evidence-based feedback. An advanced life-sciences, pharmacy or medical degree, or equivalent depth of authoring experience, is preferred. You don’t have to match every requirement exactly. We welcome applicants with different backgrounds, levels of experience and transferable skills. Pay and working arrangements Remote contractor work paying $30–$60 per hour. Weekly hours are not specified in the listing. What happens next Apply through Find Jobs in AI with your profile and CV. We’ll review your application and, if you’re a good fit, we’ll be in touch about the next steps.