Roles: Support the preparation, drafting, editing, and finalising of documents used in clinical studies and regulatory submissions.
Contract length: Full time, with training provided.
Rate: Competitive entry-level rate, details shared upon application.
Skills/background needed: No prior experience necessary. A willingness to learn document preparation, attention to detail, and basic comfort with word processing tools such as Microsoft Word and Google Docs are all you need to get started.
Location: Remote work worldwide (United States preferred)
This is a fully remote, work-from-home role open to beginners. You will help draft and edit study documents, keep review timelines on track, and support team meetings. Full training is provided, so you can build these skills as you go. You will also help with peer review and editing support for other documents, and learn to follow standard processes and templates.
You will work closely with cross-functional teams and build effective working relationships. Opportunities for growth are available as you develop in the role. If you are organised, curious, and ready to learn, this is a great place to start.
Ready to get started? Submit your application below.