Lisa Cuff
About Lisa Cuff
Lisa Cuff is a Protocol Specialist at Bristol-Myers Squibb in New Jersey with over 25 years of experience in the pharmaceuticals industry, including extensive expertise in clinical trial management and protocol compliance.
Current Position at Bristol-Myers Squibb
Lisa Cuff is currently employed as a Protocol Specialist at Bristol-Myers Squibb in New Jersey, United States. In this role, Lisa is responsible for managing clinical trial protocols and ensuring compliance with regulatory standards. Her expertise in these areas positions her as an integral part of the team at Bristol-Myers Squibb.
Previous Roles at Bristol-Myers Squibb
Lisa Cuff has a long tenure with Bristol-Myers Squibb, spanning over 18 years. She initially joined the company as a Senior Clinical Trials Associate, a position she held from 2004 to 2015. She then transitioned to the role of Project Clinical Trials Associate from 2015 to 2017. These roles allowed her to develop a strong skill set in clinical trial coordination and protocol management.
Experience at Bayer Healthcare
Before joining Bristol-Myers Squibb, Lisa Cuff worked at Bayer Healthcare as a Senior Administrative Assistant for nine years, from 1995 to 2004. Located in Berlin, Germany, this role provided her with a solid foundation in administrative support, which she later leveraged in her clinical trials career.
Education and Business Administration Background
Lisa Cuff studied Business Administration at Albertus Magnus College, where she achieved her Associate's degree from 2004 to 2006. Her education in business administration has been instrumental in her ability to manage administrative tasks and clinical trial protocols efficiently.
Over 25 Years of Pharmaceuticals Industry Experience
With over 25 years of experience in the pharmaceuticals industry, Lisa Cuff has built a career characterized by her extensive knowledge and expertise in clinical trial protocol management and regulatory compliance. Her career trajectory includes a pivotal transition from administrative support to a focus on clinical trials, showcasing her versatility and depth of experience.