Kimberly Newman

Kimberly Newman

Executive Director, Launch Excellence @ Bristol Myers Squibb

About Kimberly Newman

Kimberly Newman is the Executive Director of Launch Excellence at Bristol Myers Squibb, with extensive experience in project management, strategy, and operations across various roles in the pharmaceutical and consulting industries.

Current Role at Bristol Myers Squibb

Kimberly Newman is currently serving as the Executive Director of Launch Excellence at Bristol Myers Squibb in Princeton, New Jersey. In this role, she is responsible for overseeing the launch excellence team, ensuring that product launches align with the company's strategic vision and operational capabilities.

Previous Roles at Bristol Myers Squibb

Before her current position, Kim worked as the Senior Director of Portfolio Strategy & Medical Launch Excellence at Bristol Myers Squibb in Princeton, NJ. She also served as the Director - Business Operations Lead for European Markets, Australia, and Canada Medical from 2017 to 2022. From 2011 to 2024, she was the Director of Strategy & Operations/Project Management. Additionally, she held the role of Associate Director - Project Manager from 2009 to 2011.

Work Experience at Deloitte and Aventis

Kimberly has also worked at Deloitte as a Senior Consultant/Program Management Office Lead from 2006 to 2008. Prior to Deloitte, she was the Global Head North American GPE/Regulatory Information Systems at Aventis from 2000 to 2003.

Educational Background

Kimberly Newman holds a Master of Business Administration (MBA) in Business Administration and Management, General from Rutgers University - Newark, achieved between 2011 and 2013. She also earned a Master's Certificate in Project Management from Stevens Institute of Technology in 1997-1998. Additionally, she holds a Bachelor’s Degree in English Language and Literature, General from Thomas Edison State University.

Skills and Expertise in the Pharmaceutical Industry

Kimberly has extensive experience with 21 CFR Part 11 compliance, crucial for electronic records and electronic signatures in the pharmaceutical industry. She has a strong background in process engineering and solutions implementation, which has been instrumental in her roles. Kimberly has led global cross-functional project teams, managed vendor and contract relationships, and has demonstrated abilities in translating strategy into operations. Her experience in turnaround, change management, and risk management shows her capability to handle complex and dynamic business environments.

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