Jyoshna Bagde
About Jyoshna Bagde
Jyoshna Bagde is a Senior Clinical Site Monitor at Bristol-Myers Squibb, with over a decade of experience in clinical research and data quality management.
Current Role at Bristol-Myers Squibb
Jyoshna Bagde currently holds the position of Senior Clinical Site Monitor at Bristol-Myers Squibb in New York, New York, United States. This role involves overseeing clinical trial sites to ensure compliance with protocols, regulatory requirements, and good clinical practice guidelines. She has been in this role since August 2017.
Previous Roles at Bristol-Myers Squibb
Before her current role, Jyoshna Bagde served in various capacities at Bristol-Myers Squibb. Between 2013 and 2017, she worked as a Senior Site Monitor and Clinical Data Quality Manager in New York. Additionally, she was a Clinical Research Associate and Unblinded Monitor from 2009 to 2010 in Bombay, Maharashtra, India. She also held the position of Junior Clinical Research Associate and Unblinded Monitor from 2007 to 2009.
Educational Background
Jyoshna Bagde holds a Master of Science degree, obtained between 2005 and 2007. Prior to that, she earned her Bachelor of Science degree from Patkar College of Arts & Commerce, where she studied from 2002 to 2005.
Experience at Bristol-Myers Squibb
Jyoshna Bagde has been with Bristol-Myers Squibb for over a decade, having started her tenure in 2007. Her extensive experience includes roles such as Clinical Research Associate, Unblinded Monitor, Clinical Data Quality Manager, and Senior Site Monitor. She has worked in both the United States and India, contributing significantly to various clinical research and data quality management projects.
Clinical Research and Data Quality Management
Jyoshna Bagde's background includes extensive experience in clinical research and data quality management. Over the years, she has played crucial roles in ensuring that clinical trials meet regulatory and protocol requirements. Her work has involved a strong focus on maintaining the integrity and quality of clinical data across various projects.