Bristol Myers Squibb is seeking a regulatory documentation lead to drive end-to-end workstreams for submissions and eDMS processes. You will coordinate internal teams and external authors, ensuring submission readiness across HA activities and complex protocol documents.
This role emphasizes accuracy, collaboration, and timely delivery with a focus on continuous improvement in publishing regulatory documents for general filings.
📌 Global Regulatory Documentation Leader (Bogotá)
🏢 Nutanix
📍 Bogotá
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