Diane Healey
About Diane Healey
Diane Healey is the Study Director of Oncology Global Clinical Research at Bristol-Myers Squibb in New York, with over a decade of experience in oncology research and a career spanning more than 25 years in the pharmaceutical industry.
Current Role
Diane Healey is currently serving as the Study Director for Oncology Global Clinical Research at Bristol-Myers Squibb. Based in New York, New York, United States, she oversees the planning, coordination, and execution of global clinical trials in oncology. Her role involves extensive collaboration with cross-functional teams to ensure the successful management and completion of clinical research studies.
Previous Experience at Pfizer
Diane Healey worked at Pfizer from 2000 to 2010, serving as Director. During her tenure, she was responsible for overseeing various aspects of oncology clinical development. Her role included designing and implementing clinical strategies, managing research projects, and ensuring compliance with regulatory requirements.
Legacy at Bristol-Myers Squibb
Diane Healey has a long-standing association with Bristol-Myers Squibb, having worked there for a cumulative total of over 25 years. She started her career at the company in 1988 as a Clinical Oncology Manager, a role she held until 2000. She rejoined the company later and has since been involved in leading global clinical research in oncology.
Educational Background
Diane Healey holds a Master of Science from Rensselaer Polytechnic Institute at Hartford, completed between 1996 and 2000. She also received her Bachelor of Science degree from St. John's University. Her educational background in science has laid a strong foundation for her extensive career in oncology clinical research.
Expertise in Oncology Clinical Research
Diane Healey has more than a decade of experience specifically in oncology global clinical research. She has managed numerous clinical trials and research projects, playing a pivotal role in advancing oncology therapies. Her extensive experience in this domain includes designing clinical strategies, coordinating with international teams, and ensuring regulatory compliance.