Lead Medical Writer & Regulatory Submissions Expert

A clinical research organization is seeking a Senior Medical Writer responsible for leading the development of clinical documents for regulatory submissions. This role involves managing project timelines, ensuring high-quality output, and acting as the primary client contact. The ideal candidate will possess a Bachelor’s degree in Life Sciences or related fields, have excellent communication and organizational skills, and experience in clinical research. This position is based in Cheyenne, Wyoming. #J-18808-Ljbffr