Roles: Support the planning, writing, review, and finalisation of clear, accurate clinical and regulatory documents for development programmes.
What you’ll do:
Help draft and organise scientific and technical content into well-structured documents. Perform quality checks and editorial reviews for accuracy, consistency, and clarity. Coordinate document review workflows so deadlines are met. Turn complex scientific and clinical information into clear, concise communications for a range of audiences. Work closely with teams across the business to keep documents aligned and on schedule.
Skills/background needed: No prior experience required – full training is provided. A degree in a life sciences or related field is helpful, along with strong written communication and attention to detail. Comfort using Microsoft Word, Google Docs, and collaborative authoring tools. Willingness to learn scientific and research principles and document workflows.
Contract length: Full time, remote
Rate: Competitive entry-level rate, details shared upon application.
Location: Remote work worldwide (United States preferred)
Ready to get started? Submit your application below.