Roles: Clinical and regulatory writing support
We are looking for a beginner-friendly writer to help prepare clinical and regulatory documents for study teams. This is a fully remote, work-from-home role with full training provided — no prior experience is required to get started.
What you will do:
• Draft and revise study documents in partnership with team members
• Help review and summarise study data and answer team questions
• Keep related documents consistent and well organised
• Support the development of clear project plans and processes
Skills/background needed:
• Strong written and spoken communication
• Willingness to learn document preparation and editing
• Comfortable working with standard word processing and templates
• Organised, self-sufficient, and open to mentoring on new tasks
Rate: Competitive entry-level pay, details shared upon application.
Contract length: Full time, flexible remote work
Location: Remote work worldwide (English speaking preferred)
Ready to get started? Submit your application below.