We’re looking for an entry-level Medical Writer to join our team and help create clear, accurate regulatory documents that support drug development and approval processes. You’ll work fully remote from anywhere in the world, collaborating with experienced colleagues to develop your expertise in medical writing and regulatory standards.
What you’ll do:
• Write and edit clinical study documents, including protocols, clinical study reports, safety summaries, and regulatory submissions
• Follow established regulatory guidelines and company standards to ensure all documents are accurate, clear, and compliant
• Coordinate reviews with team members and clients to refine documents
• Perform literature searches and manage source documentation properly
• Work with colleagues in data management, biostatistics, and regulatory affairs to produce high-quality deliverables
• Learn regulatory requirements and industry standards through hands-on experience and training
Skills/background needed:
• Strong writing and communication skills
• Attention to detail and ability to follow guidelines and templates
• Basic project management and time management abilities
• Willingness to learn regulatory standards and medical writing best practices
• Ability to work collaboratively with a team
• No prior medical writing experience required – full training provided
Rate: Competitive entry-level pay, details shared upon application.
Contract length: Permanent
Location: Remote work worldwide (English speaking preferred)
Ready to get started? Submit your application below.