We are looking for a detail-oriented Medical Writer to join our team and help develop clinical and regulatory documents for pharmaceutical, biotech, and medical device programmes. This is a fully remote role perfect for someone with strong writing skills and an interest in healthcare documentation.
What you’ll do:
Write and edit clinical, safety, and regulatory documents including study protocols, reports, patient summaries, and submission-level materials. Collaborate with cross-functional teams including clinical, data management, and regulatory specialists. Manage project timelines and client communications. Review documents for accuracy, consistency, and adherence to industry standards. Support quality control processes and maintain detailed audit trails. Assist with administrative tasks such as timeline tracking and meeting coordination.
Skills/background needed:
Bachelor’s degree (preferably in a science or medical field). Strong writing and editing skills with expert proficiency in Microsoft Word. Understanding of clinical research principles and regulatory guidelines. Excellent attention to detail, project management abilities, and communication skills. Ability to work independently and manage multiple deliverables simultaneously. Familiarity with regulatory submission processes is helpful but not essential—full training will be provided.
Contract length: Full time, permanent
Rate: Competitive entry-level pay, details shared upon application.
Location: Remote work worldwide (English speaking preferred)
Ready to get started? Submit your application below.