Medical Writing Consultant

Job Summary

A company is looking for a Consultant I, Medical Writing.

Key Responsibilities

• Author regulatory documents including Clinical Study Reports and submission materials
• Lead the development of complex regulatory modules and ensure document accuracy
• Coordinate regulatory projects and maintain strong client relationships

Qualifications and Requirements

• Advanced degree in a life or health science discipline preferred
• Strong foundation in medical and regulatory writing
• Exceptional project and time management skills
• Proficiency in Microsoft Office Suite and familiarity with regulatory document management systems
• Experience with regulatory submissions and understanding of global regulatory standards