Daniel Pérez Arango is a Sr. Associate Director in Clinical Trial Management at Medpace, where they foster collaboration among investigators, clinical sites, and vendors across the Americas. With over two years in this role, Daniel emphasizes resource flexibility, risk management, and process enhancement while ensuring operational excellence. They have previously held significant positions at Bristol-Myers Squibb, Roche Pharmaceuticals, and Novartis, showcasing extensive experience in clinical trial oversight, quality management, and project execution. Daniel is a certified Clinical Research Professional (CCRP) and has acquired multiple degrees, including an MBA and a specialization in Pharmaceutical Marketing.
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