Oncology Medical Writer

Job Summary

To support a growing oncology practice, the full-time Principal Medical Writer will independently author and manage clinical program documents, lead cross-functional coordination, and ensure timely delivery of high-quality medical writing deliverables in a remote environment.

Key responsibilities

• Independently authors and manages clinical and regulatory documents, ensuring adherence to regulatory standards
• Leads cross-functional coordination of resources to manage medical writing and quality control deliverables
• Supervises and mentors less experienced medical writers while managing client expectations and project timelines

Required qualifications

• Bachelor's degree or higher in a medical or scientific discipline
• Minimum of 7 years of experience in writing clinical and/or regulatory documents for drugs, biologics, or medical devices
• Advanced knowledge of clinical research principles and regulatory submission requirements
• Proficiency in MS Word with strong project management skills
• Experience in relationship building and strategic collaboration with key business accounts