Jen Roden

Jen Roden

Senior Clinical Trial Monitor @ Bristol Myers Squibb

About Jen Roden

Jen Roden is a Senior Clinical Trial Monitor at Bristol Myers Squibb in San Diego, California, with over 16 years of experience in clinical research and trial monitoring.

Current Position at Bristol Myers Squibb

Jen Roden is currently a Senior Clinical Trial Monitor at Bristol Myers Squibb, located in San Diego, California, United States. She transitioned to this role in October 2021. In this position, she oversees and coordinates clinical trials to ensure compliance with regulatory requirements and standard operating procedures.

Previous Experience at PRA Health Sciences

Prior to her current role, Jen worked as a Clinical Research Associate at PRA Health Sciences from 2015 to 2021, based in Seattle, Washington. Her tenure at PRA Health Sciences lasted six years, during which she was responsible for monitoring clinical trials, ensuring data integrity, and managing site relationships.

Roles at University of Washington

Jen Roden spent a significant portion of her career at the University of Washington, holding various roles for a total of 10 years. She served as a Research Program Manager from 2014 to 2015 in the Greater Seattle Area, a Research Manager from 2009 to 2014, and a Clinical Research Coordinator from 2005 to 2009. Her responsibilities included managing research programs, coordinating clinical trials, and overseeing research staff.

Educational Background

Jen Roden studied at the University of Washington, where she gained the education necessary to support her extensive career in clinical research and trial monitoring. Her academic foundation has been instrumental in her various research and management roles.

Experience in Clinical Research and Trial Monitoring

With over 16 years of experience, Jen Roden has a robust background in clinical research and trial monitoring. Her career spans both academic and industry settings, providing her with comprehensive expertise in managing and coordinating clinical trials. She has worked extensively in roles that require strong organizational skills and attention to regulatory compliance.

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