Susan Werner
About Susan Werner
Susan Werner is a Clinical Site Monitor at Bristol-Myers Squibb with over 9 years of experience in clinical site monitoring and regulatory compliance.
Title and Current Position
Susan Werner is a Clinical Site Monitor currently working at Bristol-Myers Squibb. In her role, she focuses on overseeing clinical trial sites, ensuring compliance with protocols and regulatory requirements.
Previous Positions and Experience
Before joining Bristol-Myers Squibb, Susan Werner worked as a Senior Clinical Research Associate at ICON PLC from 2011 to 2014 in Düsseldorf, Nordrhein-Westfalen, Germany. Prior to that, she was a Clinical Research Associate II at RPS Nürnberg in 2011 for 7 months. She also worked at Chiltern as a Clinical Research Associate from 2008 to 2010 for 2 years.
Experience in Clinical Site Monitoring
Susan Werner has over 9 years of experience in clinical site monitoring at Bristol-Myers Squibb. She has worked on multiple clinical trials across various therapeutic areas, gaining extensive experience in regulatory compliance and site management. Her background includes managing clinical trial documentation and ensuring adherence to Good Clinical Practice (GCP) guidelines.
Training and Mentoring
Susan Werner has participated in the training and mentoring of junior clinical research associates. Her experience and knowledge make her a valuable resource for new team members, helping them understand the complexities of clinical site monitoring and adherence to regulatory standards.