Marie Swinarski
About Marie Swinarski
Marie Swinarski is a Clinical Research Associate at Bristol-Myers Squibb, with over a decade of experience in clinical research and a strong academic background from German universities.
Current Role at Bristol-Myers Squibb
Marie Swinarski is currently working at Bristol-Myers Squibb as a Clinical Research Associate - CH. She has been with the company for more than six years, demonstrating a significant commitment to the organization. Her role involves managing and monitoring clinical trials to ensure they comply with regulatory requirements and meet the company's standards.
Previous Experience at Bristol-Myers Squibb
Before her current role, Marie Swinarski worked as a Clinical Research Associate - GER at Bristol-Myers Squibb for 11 months from 2015 to 2016. Her transition from a Germany-based position to a Switzerland-based role reflects her adaptability and expertise in clinical research across different regions.
Experience at Max Delbrück Center
Marie Swinarski has extensive research experience from her time at the Max Delbrück Center in Berlin, Germany. She worked there as a Graduate Research Assistant from 2011 to 2015, following her tenure as a Research Assistant from 2010 to 2011. During her four years as a Graduate Research Assistant, she gained valuable insights and hands-on experience in scientific research.
Academic Background
Marie Swinarski has a robust academic background with degrees from three prestigious German universities. She earned her Doctor of Philosophy (Ph.D.) from Humboldt University of Berlin between 2011 and 2016. Prior to that, she obtained her Master of Science degree from Kiel University from 2008 to 2011. She began her academic journey with a Bachelor of Science from Freie Universität Berlin, completed between 2005 and 2008.
Early Career and Research Experience
Marie Swinarski began her career in research as an Undergraduate Research Assistant at the Zentrum für Integrative Psychiatrie from 2009 to 2010. She further gained experience as a Clinical Trial Monitor and CRA, roles that equipped her with the skills necessary for overseeing clinical trials and ensuring their compliance with established protocols.