Sheryl Beauchamp
About Sheryl Beauchamp
Sheryl Beauchamp is the Director of Project Management at Bristol Myers Squibb, with over 15 years of experience in the pharmaceutical and biotech industries.
Company
Sheryl Beauchamp is currently employed at Bristol Myers Squibb, serving as the Director of Project Management. Bristol Myers Squibb is a leading biopharmaceutical company, and in her role, Sheryl likely manages projects that span from early drug development through to commercialization, ensuring alignment with company goals and regulatory requirements.
Title
Sheryl Beauchamp holds the position of Director of Project Management at Bristol Myers Squibb. In this capacity, she oversees project planning, execution, and delivery, working closely with cross-functional teams to achieve project milestones while maintaining compliance with industry standards and regulations.
Education and Expertise
Sheryl Beauchamp holds a Bachelor's degree in Chemical Engineering with a minor in Biochemical Engineering from Stevens Institute of Technology. She also earned a Graduate Certificate in Pharmaceutical Manufacturing from the same institution. Sheryl specializes in Electronic Data Capture (EDC) planning and implementation, safety reporting, and clinical data flow design. Her expertise includes developing support and operating models for pharmaceutical R&D and focusing on process optimization and roadmap design strategy.
Work History
Sheryl Beauchamp has a robust work history in the pharmaceutical and biotech industries. Before joining Bristol Myers Squibb, she was the Director of Project Management Drug Safety at Celgene from 2017 to 2019. Prior to that, she had multiple roles at Eisai US, including Associate Director of Strategic Planning & Portfolio Management / Medical Solutions (2015-2017) and Associate Director of Clinical Solutions Architect (2014-2015). She spent nine years at Accenture focusing on Pharma R&D, after early career roles at ImClone Systems, Boston Scientific, and Ethicon. Her extensive experience covers both strategic planning and system implementation projects.
Experience in Pharma and Biotech
With over 15 years of experience in the pharmaceutical and biotech fields, Sheryl Beauchamp has developed a profound understanding of the industry. Her career spans through strategy and system implementation roles, offering insights into safety reporting, clinical data flow design, and process optimization. She has contributed significantly to the development and execution of electronic data capture systems and has led projects aimed at enhancing efficiency and compliance within R&D environments.