Join a growing team supporting the development and approval of healthcare products. In this remote role, you will author and oversee regulatory submission documents, lead writing activities for complex product applications, and mentor junior writers.
What you will do:
You will prepare regulatory documents including clinical study reports, investigator guidance, protocols, consent forms, and briefing materials. You will conduct formal reviews of documents following standard procedures, lead writing activities for new and supplemental applications, serve as a subject-matter expert on product teams, supervise contract writers, and mentor junior team members. You will also help generate document timelines and support departmental initiatives.
Skills/background needed:
You should have experience in medical writing, regulatory affairs, research, or a related field. Prior experience in biotech or pharmaceutical documentation is helpful but not required. We provide full training and support—this role welcomes candidates ready to grow into the position and learn on the job.
Rate: Competitive entry-level pay, details shared upon application.
Contract length: Ongoing
Location: Remote work worldwide (English speaking preferred)
Ready to get started? Submit your application below.