We are looking for a Medical Writer to join a remote, full-time team working on regulatory writing projects in the oncology therapeutic area. This is a beginner-friendly role with full training provided, so no prior experience is required.
Roles: Support writing projects under the guidance of senior writers, help prepare clinical study protocols, clinical study reports, and patient narratives, review statistical analysis plans and table and figure specifications, and coordinate with data, biostatistics, regulatory, and medical teams. You will follow established regulatory standards and the onboarding process.
Rate: Competitive entry-level rate, details shared upon application.
Contract length: Full-time, ongoing
Skills/background needed: A bachelor’s degree (science or arts) or equivalent practical experience, strong English grammar and proofreading skills, comfort with Microsoft Word, Excel, and PowerPoint, and a willingness to learn. Full training is provided.
Location: Remote work worldwide (United States preferred)
Ready to get started? Submit your application below.