Roles: Support the preparation and review of scientific and medical documents, including clinical study reports, protocols, and safety summaries. Help draft scientific communication materials such as manuscripts, abstracts, and educational content. Assist with formatting, proofreading, and version control using templates and style guides. Keep document timelines updated and help coordinate review comments among team members.
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 keen eye for detail, clear writing skills, and a willingness to learn are all you need. Comfortable using Microsoft Word, Google Docs, and email. You will be supported as you build familiarity with scientific and regulatory documents.
Location: Remote work worldwide (English speaking preferred)
This is a fully remote, work-from-home role. You will work from anywhere and collaborate with a supportive team through online tools. Opportunities for growth are available as you develop your skills.
Ready to get started? Submit your application below.