Medical Writer

Job Summary

To support clinical research initiatives, the full-time remote Medical Writer will author clinical trial and regulatory documents, engage with cross-functional teams, and ensure document quality and compliance.

Key responsibilities

• Author clinical trial and regulatory documents according to specified templates and guidelines
• Coordinate quality control processes for all documents produced
• Collaborate with cross-functional teams to develop clear and compliant documentation

Required qualifications

• Master's degree with at least 5 years of medical writing experience in the Biotech/Pharmaceutical industry, or a Bachelor's degree with at least 8 years of relevant experience
• Proven ability to understand and interpret data for practical application
• Advanced knowledge of scientific and technical writing and editing
• Strong time and project management skills
• Experience in a collaborative team environment