Renee Evens
About Renee Evens
Renee Evens is a Senior Global Clinical Trial Manager at Bristol Myers Squibb with over 20 years of experience in clinical research and quality assurance roles.
Current Role at Bristol Myers Squibb
Renee Evens currently serves as the Senior Global Clinical Trial Manager at Bristol Myers Squibb. She has been with the company since January 2017, bringing over six years of experience to her current role. Her responsibilities involve managing global clinical trials, ensuring compliance with regulatory requirements, and overseeing the overall progress and quality of clinical research projects.
Previous Experience at Advanced Clinical and ImClone Systems
Before her current position, Renee Evens worked at Advanced Clinical as an Expert Clinical Manager II from 2015 to 2016. She also held the position of Clinical Trial Manager at ImClone Systems, a wholly-owned subsidiary of Eli Lilly and Company, from 2014 to 2015. In both roles, she focused on clinical trial management, which included planning, execution, and monitoring of clinical studies.
Career at LifeCell Corporation and Reckitt Benckiser
Renee Evens spent five years at LifeCell Corporation as a Senior Clinical Project Manager from 2008 to 2013, where she managed complex clinical projects and ensured adherence to quality standards. Additionally, she worked briefly at Reckitt Benckiser as a Global Clinical Trial Manager in 2013, further expanding her expertise in global trial management.
Early Career in Quality Assurance and Clinical Research
Renee Evens' career began with roles focused on quality assurance and clinical research. She worked at Medarex Inc. as a Quality Assurance Associate I – Batch Record Reviewer from 2002 to 2003 before transitioning to a Clinical Research Associate II position. She also served as a Senior Auditor, Clinical QA at Covance Inc. from 2006 to 2007 and as a Consultant Clinical Research Associate at Cordis Corporation from 2007 to 2008.
Educational Background and Skills
Renee Evens holds a Bachelor of Arts degree in Biology from Kean University. She has over 20 years of experience in clinical research and quality assurance roles. Her diverse skill set includes expertise in quality control, clinical trial management, and regulatory compliance, making her a valuable asset in the clinical research field.