Stephanie K.
About Stephanie K.
Stephanie K. is the Associate Director, Senior Clinical Scientist at Bristol Myers Squibb, with extensive experience in clinical trial management and medical imaging in oncology trials.
Current Role at Bristol Myers Squibb
Stephanie K. holds the position of Associate Director, Senior Clinical Scientist at Bristol Myers Squibb. In this capacity, she is responsible for various high-level clinical and scientific tasks, including overseeing protocol development, managing clinical trial documentation, and serving as the primary clinical contact for protocol issues in clinical trials.
Experience at Bristol Myers Squibb
Stephanie K. has a longstanding career at Bristol Myers Squibb, having transitioned through multiple roles since 2015. She started as a Clinical Site Manager and progressed to the roles of Sr Global Trial Manager/Sr Clinical Protocol Manager, and Clinical Scientist. Her extensive experience spans across clinical trial management, documentation oversight, and the implementation of automated randomization methodologies.
Past Positions at PAREXEL
Before her tenure at Bristol Myers Squibb, Stephanie K. worked at PAREXEL in various capacities including Project Manager and Live Study Manager. Her responsibilities included managing clinical projects and coordinating automated supplies management in clinical trials. She worked at PAREXEL from 2010 to 2015, culminating her experience as a Senior Clinical Project Associate.
Educational Background
Stephanie K. has a comprehensive educational background in the fields of biology, medical pharmacology, and clinical trial sciences. She holds a Bachelor of Arts in Biology from Arcadia University and a Master of Science in Clinical Trial Sciences from Rutgers, The State University of New Jersey-Newark. Additionally, she studied Medical Pharmacology and Therapeutics at the University of Florida.
Clinical Trial Expertise
Stephanie K. has considerable expertise in managing and leading various aspects of clinical trials. She is proficient in imaging criteria including RECIST, RANO, CHESON, WHO, and PET imaging. She has led medical imaging for global oncology trials and ensures compliance with regulatory requirements and ICH/GCP guidelines. Her duties also encompass the oversight of Trial Master File management and independent review processes in clinical trials.