Tammy Ramirez

I am a results-oriented senior supply chain leader with 15+ years in biotech and pharmaceutical clinical trial supply management, focused on end-to-end strategies, vendor relations, and global logistics.

I have developed and executed supply strategies across Early Phase I through Phase III trials, managed small and large molecule products (oral and injectable), and led IRT/IVRS setups including specifications review and UAT to optimize resupply and inventory.

My work emphasizes regulatory compliance (GMP, GCP, GDP), import/export coordination, forecasting, and risk mitigation to ensure on-time delivery and inspection readiness; I have authored cGMP documentation, SOPs, change controls, and CAPAs.

I lead cross-functional teams, mentor direct reports, and drive process improvements that reduce risk and improve operational efficiency while partnering closely with Clinical Operations, QA, Regulatory Affairs, CMOs, CROs, depots, and logistics providers.