Violeta Tahuilan
About Violeta Tahuilan
Violeta Tahuilan is the Leader of the Rco and Grs Work Stream at Bristol-Myers Squibb, overseeing the implementation of the new EU Clinical Trial Regulation. She has extensive experience in clinical site management and regulatory operations, with a diverse educational background.
Current Role at Bristol-Myers Squibb
Violeta Tahuilan currently holds the position of Leader of the Rco and Grs Work Stream in Charge of the Implementation of the New EU CT Regulation at Bristol-Myers Squibb in New Jersey, United States. Her role focuses on overseeing the regional clinical operations and regulatory adherence to new European Union clinical trial regulations.
Previous Positions at Bristol-Myers Squibb
Prior to her current role, Violeta served in various capacities at Bristol-Myers Squibb, including Manager of Local Clinical Research Project Managers. Her extensive work at the company encompasses over nine years of experience in clinical site management, and she has also held the position of Associate Director, Manager of Clinical Site Management in New Jersey.
Experience at MSD
Before joining Bristol-Myers Squibb, Violeta Tahuilan was the Oncology Director at MSD, where she worked in the Global Clinical Trials Operations (GCTO) Department in Spain. Her tenure at MSD included significant responsibilities in oncology research management, contributing to clinical trials and regulatory processes.
Educational Background
Violeta Tahuilan has a diverse educational background. She studied Nutrition and earned a Master's degree between 2013 and 2014. She also attended Universidad Pedagógica Nacional from 1994 to 1998 and studied Education from 1992 to 1993. Her earlier education includes a two-year study of English, Italian, and French languages at Universidad Motolinía, A.C., from 1990 to 1992.