Brenda Mercier
About Brenda Mercier
Brenda Mercier is a Clinical Site Monitor at Bristol-Myers Squibb in New York with over 20 years of experience in clinical site monitoring and a strong background in clinical research and site management.
Title
Brenda Mercier currently holds the position of Clinical Site Monitor. She is employed at Bristol-Myers Squibb in New York, New York, United States.
Company
Brenda Mercier has been employed at Bristol-Myers Squibb for over two decades. She is based in New York, New York, where she works as a Clinical Site Monitor. Bristol-Myers Squibb is a global biopharmaceutical company known for its focus on delivering innovative medicines that help patients prevail over serious diseases.
Education and Expertise
Brenda Mercier earned her Bachelor's degree from Simon Fraser University, where she studied from 1989 to 1993. Prior to that, she attended Vanier College from 1973 to 1976. She has over 20 years of experience in clinical site monitoring, signaling a deep expertise in the field of clinical research and site management.
Background
Before her tenure at Bristol-Myers Squibb, Brenda Mercier worked at VGH as a CVA Clinical Trials Study Coordinator from 1995 to 2002. During her 7 years at VGH, she was involved in clinical trials for cardiovascular diseases. Over the course of her career, she has developed extensive experience in coordinating clinical trials and ensuring compliance with regulatory requirements.
Clinical Research Experience
With over two decades at Bristol-Myers Squibb, Brenda Mercier has accumulated significant expertise in the field of clinical site monitoring. Her role involves coordinating clinical trials, ensuring that all processes adhere to stringent regulatory standards, and maintaining the integrity and accuracy of clinical data. Her background at VGH and deep experience in the field make her well-versed in the intricacies of clinical research.