Brad Lavinder

Brad Lavinder

Associate Director @ Aimmune Therapeutics

About Brad Lavinder

Brad Lavinder is an Associate Director at Aimmune Therapeutics, where he has worked since 2020. He has extensive experience in clinical supply chain management, having held various roles in the pharmaceutical industry over the past two decades.

Work at Aimmune Therapeutics

Brad Lavinder has been serving as Associate Director at Aimmune Therapeutics since 2020. In this role, he oversees various aspects of clinical supply management, including the development of metrics to monitor performance related to clinical trial inventory and planning. He previously held the position of Sr. Manager, Clinical Supply Chain Operations at Aimmune Therapeutics from 2018 to 2020, where he contributed to the automation of the distribution of investigational medicinal products. His work is based in North Carolina, United States.

Previous Experience in Clinical Supply Management

Before joining Aimmune Therapeutics, Brad Lavinder worked at Almac Group as a Global Project Leader/Supply Chain Manager from 2014 to 2018. He also held the position of Clinical Supply Manager at UCB Pharma for one year in 2004. His experience includes roles at UCB as Clinical Supply Program Manager from 2006 to 2013 and Clinical Supply Coordinator at Schwarz Biosciences from 2006 to 2007. He has a comprehensive background in clinical supply chain operations.

Education and Expertise

Brad Lavinder earned a Bachelor of Science degree in Exercise Science and Physiology from Appalachian State University, where he studied from 1993 to 1997. His expertise includes developing IXRS systems and collaborating with Clinical Operations and external vendors. He has a strong focus on automating the distribution of investigational medicinal products and managing global labeling for multi-national clinical studies.

Background in Clinical Operations

Brad Lavinder began his career as a Medical Lab Technician at UNC Hospitals from 1997 to 1998. He transitioned to roles in clinical operations, including Clinical Endpoint Validation Specialist II at Quintiles from 2005 to 2006. His extensive experience in clinical supply management spans over two decades, with a focus on optimizing business needs and budget through vendor management and contract negotiations.

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