Women in Leadership Advisory Member |
MaryLou Schoonover
Active Term: 10/2024 - 10/2025
Areas of Expertise
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Sr. Mgr., Customer Due Diligence & State Licensing, DEA ComplianceEndo USA, IncMary-Lou Schoonover currently serves as the Customer Due Diligence and State Licensing Senior Manager of the DEA Compliance Team for Endo USA, Inc. She is responsible for the licensing of all the U.S. based Endo facilities as well as the DEA Suspicious Order Monitoring and Customer Due Diligence program. Mary-Lou has over 25 years of combined experience between Prescription Drug Marketing Act (PDMA) and DEA compliance in the pharmaceutical industry.
She has previously worked for MedPro Systems, Allergan (formerly Actavis), Reckitt Benckiser, and the United States Pharmacopeia. Considered a subject matter expert in State Licensing, PDMA and DEA Compliance, Mary-Lou attributes her wealth of knowledge and professional success to the individuals she has worked with throughout her career. She has a Bachelor of Science in Business Administration and Management from Centenary University and is a graduate of the National Academy of Paralegal Studies. Mary-Lou is a Certified Corporate Paralegal. She has served as an industry volunteer for various organization and is a frequent presenter at industry conferences. She is a member of or affiliated with the New Jersey Pharmacy Industry Group (NJPIG), National Association of State Controlled Substance Authorities (NASCSA), National Association of Drug Diversion Investigators (NADDI) and IQVIA. Mary-Lou was the recipient of the 2021 President’s Award from NASCSA and, the 2021 Inaugural Endo Living Our Values Award for Integrity and Quality. In her spare time, Mary-Lou volunteers for the Coalition for Safe and Healthy Families in Sussex and Warren Counties, NJ. |