Rosemarie Harris
About Rosemarie Harris
Rosemarie Harris is the Director of Drug Development, Project Management, RDSP at Bristol Myers Squibb, with over 25 years of experience in the pharmaceutical industry, focusing on drug development and project management.
Current Role at Bristol Myers Squibb
Rosemarie Harris serves as the Director of Drug Development, Project Management, RDSP at Bristol Myers Squibb. In her role, she oversees the development of new pharmaceutical drugs, ensuring that all phases of drug development are managed efficiently. Her responsibilities include coordinating cross-functional teams and ensuring that project milestones and deliverables are met.
Previous Experience at Celgene
Rosemarie Harris worked at Celgene from 2014 to 2021. She initially joined as a Senior Trial Manager in Clinical Operations for Hematology/Oncology. After two years, she was promoted to Associate Director of Project Leadership, a position she held for five years. During her time at Celgene, Harris contributed significantly to the successful launch of multiple oncology drugs and played a key role in integrating Celgene's project leadership team into Bristol-Myers Squibb following their merger.
Professional Background
With over 25 years in the pharmaceutical industry, Rosemarie Harris has amassed extensive experience in drug development and project management. She has held various positions, including Senior Protocol Manager at Bristol-Myers Squibb, Lead CRA/Project Manager at Schering-Plough Research Institute, and CRA/Outsourcing Manager at Purdue Pharma L.P. Her diverse roles have provided her with a strong foundation in clinical research activities, clinical operations, and protocol management.
Educational Background
Rosemarie Harris holds a Master's degree in Biochemistry from Stevens Institute of Technology, completed between 1995 and 1997. She also earned a Bachelor of Science (BS) in Chemistry from Manhattan College, where she studied from 1987 to 1991. Her academic background has equipped her with a solid understanding of the biochemical and chemical principles critical for her roles in the pharmaceutical industry.
Clinical Trials Expertise
Throughout her career, Rosemarie Harris has demonstrated extensive expertise in managing clinical trials, particularly in the fields of hematology and oncology. She has overseen numerous trials, ensuring they are conducted in compliance with regulatory standards and timelines. Her leadership in clinical operations has been instrumental in the successful development and launch of new pharmaceutical drugs.