Senior Medical Writer

Job Summary

To support clinical development initiatives, the full-time Senior Medical Writer will author and manage clinical regulatory documents while collaborating with various internal teams in a remote work environment.

Key responsibilities

• Author and support medical writing content for clinical protocols, Investigator Brochures, and regulatory submission documents
• Collaborate with Clinical Development, Regulatory Affairs, and other teams to ensure timely document completion
• Oversee the document preparation process, including drafting, review cycles, and quality control

Required qualifications

• PhD or advanced degree in a scientific or clinical discipline
• 4+ years of medical writing or relevant pharmaceutical industry experience, with at least 2 years in sponsor-level clinical/regulatory writing
• Previous neuroscience experience is strongly preferred
• Understanding of drug development, biostatistics, and medical terminology
• Proficiency in Microsoft Word and familiarity with document management platforms