Senior Regulatory Medical Writer

Job Summary

A company is looking for a Principal Medical Writer to provide high-quality medical and scientific writing for clinical and regulatory documents.

Key Responsibilities

• Author and provide input on clinical documents such as study reports and protocols
• Write complex clinical and scientific documents, including IBs and INDs
• Review documents prepared by junior team members and provide mentorship

Required Qualifications

• Bachelor's degree in a scientific field; advanced degree preferred
• 5+ years of relevant experience in medical writing
• Experience in the pharmaceutical or CRO industry preferred
• Additional qualifications in medical writing (AMWA; EMWA; RAC) are advantageous
• Equivalent combinations of education and experience may be considered