Diane Olmi
About Diane Olmi
Diane Olmi is the Associate Director of Global Quality, Clinical Trials Systems & Auditing QA at Bristol Myers Squibb in Montreal, Quebec, Canada, with over 20 years of experience in clinical trials and quality assurance.
Title
Diane Olmi currently holds the position of Associate Director, Global Quality, Clinical Trials Systems & Auditing QA at Bristol Myers Squibb. She operates from Montreal, Quebec, Canada, and focuses on the global quality and auditing of clinical trials systems.
Current Position at Bristol Myers Squibb
Diane Olmi is based in Montreal, Quebec, Canada, where she serves as the Associate Director, Global Quality, Clinical Trials Systems & Auditing QA at Bristol Myers Squibb. In this role, she is responsible for overseeing and ensuring quality assurance across clinical trials systems on a global scale. Her responsibilities include auditing and maintaining compliance with clinical trial standards.
Previous Roles at Bristol Myers Squibb
Diane Olmi has held various roles at Bristol Myers Squibb over more than two decades. From 2018 to 2020, she was the Regional Clinical Compliance Lead in Canada. Between 2016 and 2019, she worked as Manager- Clinical Site Monitor / Quality Specialist in the Montreal, Canada area. Prior to that, she served as a Senior Clinical Site Monitor/Quality Manager Liaison RCO Canada from 2001 to 2019.
Experience at Kells Medical Research Group
Diane Olmi began her career at Kells Medical Research Group as a Research Nurse, where she worked from 1998 to 2001 in the Montreal, Canada area. Her responsibilities included conducting clinical research and trials, laying a strong foundation for her future roles in clinical quality assurance.
Education and Expertise
Diane Olmi studied at Vanier where she completed an Associate's degree in Registered Nursing/Registered Nurse from 1983 to 1986. She has over 20 years of experience in clinical trials and quality assurance, transitioning from clinical site monitoring to managerial positions within Bristol Myers Squibb. Her robust background in clinical compliance and quality management has been a critical asset throughout her career.