Nancy Vera
About Nancy Vera
Nancy Vera is a Sr. Clinical Site Monitor at Bristol-Myers Squibb Co in Puerto Rico with over 16 years of experience in research and development, including international work.
Current Role at Bristol-Myers Squibb Co
Nancy Vera currently holds the position of Sr. Clinical Site Monitor at Bristol-Myers Squibb Co in Puerto Rico. In her role, she oversees monitoring activities for all phase I, II, and III clinical trials, ensuring compliance with Good Clinical Practice (GCP) and FDA regulations. Her responsibilities also include performing source data verification, conducting pre-study, site initiation, and closure visits, as well as identifying potential investigators for compounds under development.
Education and Expertise
Nancy Vera holds a Bachelor of Science (B.S.) and a Master of Public Health (MPH) in Epidemiology from the University of Puerto Rico. Her educational background has equipped her with extensive knowledge in public health and clinical research. She completed her studies at the University of Puerto Rico, Mayagüez Campus, and the Graduate School of Public Health.
Professional Background
Nancy Vera's professional journey includes notable positions at major pharmaceutical and healthcare companies. She worked as a Franchise Manager at Bristol-Myers Squibb PR. Inc from 1997 to 2000. Prior to that, she served as an Accounts Manager at Merck Sharp & Dohme (I.A.) Corp for eight years, from 1989 to 1997. She began her career at Triple S (Medicare Division) as a Specialist from 1987 to 1989.
Clinical Site Monitoring Experience
Nancy Vera has significant experience in clinical site monitoring, having worked in various managerial roles. She served as a Site Manager Manager in 2008 and as a Site Monitor Manager from 2005 to 2006. Throughout her career, she has been involved in handling monitoring activities for various phases of clinical trials, ensuring stringent compliance with regulatory standards.
International Research and Development
With over 16 years of experience in research and development, Nancy Vera has engaged in international work, including projects in Europe and South America. Her extensive experience in the field has provided her with a deep understanding of clinical trial processes and regulatory requirements across different jurisdictions.