Roles: Support the preparation and review of scientific and medical documents for clinical programs, including study protocols, reports, and patient-facing materials. Help maintain templates, style guides, and document quality processes, and coordinate review timelines with other teams.
Rate: Competitive entry-level pay, details shared upon application.
Contract length: Full-time, ongoing.
Skills/background needed: No prior experience required — full training provided. A clear, careful writing style and comfort organising information in Google Docs and Microsoft Word are helpful. Willingness to learn scientific and regulatory documentation standards is key. You will work closely with a supportive team and use a team chat app and a project tracking tool for daily coordination.
Location: Remote work worldwide (United States preferred)
This is a fully remote, work-from-home role with opportunities for growth and a supportive team environment. Beginners are welcome to apply.
Ready to get started? Submit your application below.