Roles: Support the writing and updating of clinical documents for product reviews and regulatory submissions, including clinical evaluation reports, post-market follow-up plans and reports, and summaries of clinical data across product families.
Rate: Competitive entry-level pay, details shared upon application.
Contract length: Full time, with training provided.
Skills/background needed: No prior experience required. Full training is provided, so a willingness to learn and an interest in clear, accurate scientific writing are what matter most. You will work with teammates across regulatory, research and development, post-market experience, and quality to keep documents aligned with recognised standards and to answer regulatory questions on time.
This is a fully remote role. You can work from home or from anywhere, with a supportive team and opportunities for growth as you build your skills in clinical writing.
Location: Remote work worldwide (United States preferred)
Ready to get started? Submit your application below.