About this opportunity
ProPharma Group lists this Senior Medical Writer: Regulatory & Clinical Lead opportunity in northern, Kentucky. Review the employer’s description below for duties, qualifications and application requirements.
Job description
ProPharma Group seeks a Principal Medical Writer to lead medical writing efforts across regulatory submissions and clinical documentation. You will author and edit complex documents, coordinate cross-functional teams, and ensure compliance with ICH and regional guidelines.
The role requires 7+ years in clinical/regulatory writing, strong communication, and project management skills, with a preference for experience in submissions for drugs, biologics, or devices. Hybrid work available.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.