Senior Regulatory Medical Writer

Job Summary

A company is looking for a Senior Regulatory Medical Writer to provide high-quality medical and scientific writing in a remote capacity.

Key Responsibilities

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

Required Qualifications

• Bachelor's degree in a scientific field; advanced degree preferred
• 5+ years of relevant experience in medical writing, preferably in the pharmaceutical/CRO industry
• Experience in a client-dedicated role or with multiple projects preferred
• Additional qualifications in medical writing (AMWA; EMWA; RAC) are advantageous
• Equivalency of education, training, and experience may be considered