AbbVie
Megan McAvoy, M.S., CCRA, currently serves as the Associate Director and Global Program Lead for Site Management and Monitoring at AbbVie, where responsibilities include leading internal and outsourced site management for clinical research studies and ensuring the integrity and quality of monitoring activities. Prior experience includes overseeing client partnerships at Syneos Health, serving as Clinical Monitoring Project Lead at Syneos Health Clinical Solutions, and operating multiple global clinical studies at Quintiles. Early career roles include Senior Clinical Research Associate at PPD and Clinical Research Associate at ICON. Megan holds a Master of Science in Biotechnology Clinical Research from The George Washington University and a Bachelor of Business Administration from the University of Wisconsin-Whitewater.
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