Bristol Myers Squibb is seeking a Manager, Global Scientific and Regulatory Documentation to lead end-to-end regulatory filings, HA responses, and complex clinical protocols, including eDMS workflows.
You will coordinate cross-functional teams and ensure submissions are ready, with a focus on document publishing across protocol and submission types.The role emphasizes strategic direction, training, and continued process improvements in regulatory documentation to support integral clinical
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📌 Global Regulatory Documentation Lead (Bogotá)
🏢 Bristol-Myers Squibb
📍 Bogotá
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