PPD
Alona Michelle Waldrop-Kelly is an experienced professional in compliance and quality assurance within the clinical research field. Currently serving as a Senior Compliance Specialist at PPD since September 2021, Alona focuses on client risk management, CRO clinical GCP quality agreements, and process improvement aligned with industry standards. Previously, Alona held roles at Battelle as a Research QA Officer, overseeing compliance for environmental health research, and at EGL Genetics as a Clinical Laboratory Quality Management Specialist. With a background in clinical research coordination at the Center for Hepatitis C and project management at Quintiles, Alona has received advanced education, including a Master of Clinical Research Administration from Trident University International. Alona’s extensive expertise spans regulatory compliance, quality management practices, and operational oversight in laboratory and clinical settings.
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PPD
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PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Their customers include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 46 countries and approximately 23,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help customers bend the cost and time curve of drug development to deliver life-changing therapies that improve health.