Avetix Bio seeks a Senior Director, Medical and Scientific Writing to lead the development of key regulatory and clinical documents. Reporting to the SVP, Regulatory, Quality and Pharmacovigilance, you will partner with Clinical, Regulatory, Quality, Medical Affairs, Commercial and CMC teams to craft strategic messages.
You will build scalable writing infrastructure, templates, and standards, manage timelines and budgets, supervise internal and external writers, and ensure global compliance with
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