Roles: Support the writing and review of clinical and regulatory documents, working closely with a friendly team on a range of documents across different therapeutic areas.
Rate: Competitive entry-level pay, details shared upon application.
Contract length: Full time, ongoing.
Skills/background needed: No prior experience required. Full training provided. Comfortable using Microsoft Word, including tables, graphs, and figures. Good attention to detail, strong time management, and clear written communication. A degree in a medical or scientific field is helpful but not essential. Willingness to learn industry guidelines and document standards as part of the onboarding process.
Location: Remote work worldwide (United States preferred)
In this beginner-welcome role, you will write and edit a variety of documents, help coordinate reviews, keep documents tidy and organised, and work with colleagues to meet timelines. You will learn to follow regulatory standards and work within set budgets and project timelines, while building skills in document quality and consistency. Experienced team members will be on hand to guide you, and there is room to grow into more complex documents over time.
This is a fully remote position, so you can work from home and enjoy flexible remote work with opportunities for growth in a supportive team environment.
Ready to get started? Submit your application below.