Bristol Myers Squibb seeks a Manager, General Scientific and Regulatory Documentation to lead end-to-end regulatory filings, HA responses, and complex clinical protocols, including eDMS processes and submission-readiness formatting across protocol and submission document types. You will coordinate cross-functional partners, train staff, and ensure quality and efficiency through publishing workflows, PDFs, and model documents, contributing to timely submissions and compliance.
📌 Global Regulatory Documentation Lead (Bogotá)
🏢 Bristol-Myers Squibb
📍 Bogotá
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