Reggie King
About Reggie King
Reggie King is a Regulatory Affairs Labeling Specialist at Bristol Myers Squibb in Lawrenceville, New Jersey, with over a decade of experience in regulatory affairs and information management within the pharmaceutical industry.
Title
Reggie King is currently serving as a Regulatory Affairs Labeling Specialist at Bristol Myers Squibb in Lawrenceville, New Jersey.
Current Position at Bristol Myers Squibb
Reggie King holds the position of Regulatory Affairs Labeling Specialist at Bristol Myers Squibb. Based in Lawrenceville, New Jersey, he focuses on managing regulatory affairs with a specialization in labeling. His role involves ensuring compliance with regulatory standards and accurate labeling of pharmaceutical products.
Previous Experience at AbbVie
Reggie King worked in AbbVie as a Clinical Documentation Specialist from 2019 to 2020. During his eight months with the company in Abbott Park, Illinois, he was involved in managing clinical documentation and maintaining meticulous records essential for regulatory submissions.
Background in Information Management
Reggie King has extensive experience in information management, demonstrated by his roles at PRA Health Sciences and Shire. From 2017 to 2018, he worked at PRA Health Sciences as an Information Management Analyst in Deerfield, Illinois, handling data management responsibilities. Prior to that, he served as a Sr Information Management Analyst at Shire from 2016 to 2017 in Bannockburn, Illinois, where he managed vital information resources.
Educational Background
Reggie King graduated from the University of Illinois at Chicago with a Bachelor of Arts (B.A.) in Pre-Law Studies. His education provided a strong foundation for his subsequent career in the pharmaceutical industry, particularly in regulatory affairs and information management.
Early Career and Roles in the Pharmaceutical Industry
Reggie King's career in the pharmaceutical industry began as a Medical Records Coordinator at Astellas Pharma from 2007 to 2008. Over the years, he has worked at several renowned pharmaceutical companies, including Abbott, Hospira, Baxalta, and Shire, in various capacities such as Regulatory Affairs Analyst, Regulatory Affairs Specialist, and Safety Data Analyst. This diverse experience has given him a robust background in regulatory affairs and clinical documentation.