Kevin Wahl
About Kevin Wahl
Kevin Wahl is the Director of R&D QMS Documentation, Global Quality at Bristol Myers Squibb, with over 15 years of experience in project management and clinical research within the pharmaceutical and medical imaging industries.
Company
Kevin Wahl is currently employed at Bristol Myers Squibb in Princeton, New Jersey, United States. His role involves overseeing R&D QMS Documentation within the Global Quality division. Bristol Myers Squibb is a renowned pharmaceutical company specializing in the development of pioneering medicines.
Title
Kevin Wahl holds the position of Director, R&D QMS Documentation, Global Quality at Bristol Myers Squibb. His responsibilities include ensuring the quality management systems documentation for R&D adheres to global standards.
Previous Positions at Bristol Myers Squibb
Before his current role, Kevin Wahl served as Risk Management Lead at Bristol Myers Squibb from 2018 to 2022 in the Greater New York City Area. Prior to that, he worked as Protocol Manager from 2016 to 2018 in Plainsboro, New Jersey. These roles involved significant management responsibilities in clinical trial oversight and risk management.
Experience at Bioclinica
Kevin Wahl has an extensive background with Bioclinica, where he worked in various capacities for approximately five years. He transitioned from Senior Clinical Project Manager (2014-2015) to Manager, Medical Affairs (2015-2016) in Princeton, New Jersey. Earlier, he was a Project Manager from 2011 to 2014 at BioClinica, Inc., showcasing his extensive expertise in clinical project management.
Roles at RadPharm and CoreLab Partners Inc
Kevin Wahl held multiple positions at RadPharm and CoreLab Partners Inc. He served as Assistant Project Manager at CoreLab Partners Inc from 2009 to 2011. At RadPharm, he was a Project Leader from 2007 to 2008 and a Project Coordinator from 2006 to 2007, indicating a strong trajectory in project management roles early in his career.
Education and Expertise
Kevin Wahl studied at The College of New Jersey from 2001 to 2005. He has over 15 years of experience in project management and clinical research within the pharmaceutical and medical imaging industries. This extensive experience has equipped him with skills in clinical trial oversight, quality management, risk management, and leadership.