Principal Medical Writer

Job Summary

A company is looking for a Principal Strategic Medical Writer (Remote).

Key Responsibilities

• Independently write clinical and regulatory documents and coordinate their review and approval
• Communicate project timelines and deliverables to team members, holding them accountable for deadlines
• Develop expert knowledge of regulations and contribute to project management and process improvements

Required Qualifications

• Bachelor's Degree or higher in a scientific discipline
• Minimum of 5+ years of experience in the bio-pharmaceutical industry
• Extensive experience writing and editing clinical documents following regulatory guidelines
• Advanced understanding of drug development, clinical research, and regulatory requirements
• Ability to manage multiple projects and collaborate with cross-functional teams