Marta Karwowska
About Marta Karwowska
Marta Karwowska is an Associate Clinical Site Manager at Bristol-Myers Squibb with over 15 years of experience in clinical research and site management.
Current Position at Bristol-Myers Squibb
Marta Karwowska is currently serving as an Associate Clinical Site Manager at Bristol-Myers Squibb. In this role, she is responsible for overseeing clinical trial sites, ensuring compliance, and managing site operations. Her extensive experience in the field allows her to effectively handle the complexities of clinical site management.
Previous Roles at Bristol-Myers Squibb
Before her current position, Marta Karwowska worked as a Clinical Site Monitor at Bristol-Myers Squibb from 2015 to 2016. Based in New York, she monitored clinical trial sites to ensure adherence to protocols and regulatory requirements. This role provided her with a solid foundation in site monitoring and paved the way for her current managerial role within the company.
Career History at PPD
Marta Karwowska spent a significant part of her career at PPD, holding multiple positions over seven years. She began as a Research Assistant from 2008 to 2009, then advanced to a Clinical Research Associate from 2009 to 2012. She continued her career progression by becoming a Clinical Research Associate II from 2012 to 2015. During her time at PPD, she gained extensive experience in clinical research and trials.
Educational Background
Marta Karwowska holds a Master of Science degree from the University of Warsaw, completed between 1998 and 2003. She furthered her education by attending the SGH Warsaw School of Economics from 2005 to 2006. Her academic background has provided her with a solid understanding of economics and science, which has been beneficial in her clinical research career.
Experience in Clinical Research and Site Management
With over 15 years of experience in clinical research and site management, Marta Karwowska has built a robust career in the industry. She has worked in various capacities, from research assistant to associate clinical site manager, and has been involved in clinical trials both in the United States and Poland. Her extensive background in clinical trials and site management showcases her expertise and dedication to the field.