Jessica (Hotter) Utzig Bs, Ccrp
About Jessica (Hotter) Utzig Bs, Ccrp
Jessica (Hotter) Utzig, Bs, Ccrp, is a Senior Clinical Trial Monitor at Bristol Myers Squibb with extensive experience in managing oncology clinical trials and a strong background in teaching and mentoring.
Current Title and Role
Jessica (Hotter) Utzig, Bs, Ccrp holds the position of Senior Clinical Trial Monitor at Bristol Myers Squibb. Her responsibilities encompass overseeing the compliance and quality of clinical trials, ensuring that all trials adhere to FDA/ICH-GCP guidelines. Her role demands a comprehensive understanding of clinical research and trial management, contributing to the company's goal of advancing life-changing treatments.
Previous Employment at Bristol Myers Squibb
Before becoming a Senior Clinical Trial Monitor, Jessica served as a Clinical Trial Monitor at Bristol Myers Squibb for 9 months, from 2020 to 2021. In this role, she was instrumental in supervising trial-related activities, ensuring protocols were followed, and maintaining the quality and integrity of the data collected. Her experience at this level has provided her a strong foundation for her current responsibilities.
Experience at Syneos Health
Jessica worked at Syneos Health initially as a CRA II and later as a Senior CRA from 2017 to 2020. In her roles, she was involved in the management and monitoring of clinical trials, primarily focusing on studies for Bristol Myers Squibb. Her tenure at Syneos Health honed her skills in clinical trial monitoring, particularly in the oncology space.
Education and Academic Background
Jessica completed her Bachelor of Science degree in Kinesiology: Exercise and Movement Science at the University of Wisconsin-Madison. She also attended the University of Minnesota for one year. Her academic journey began at Seymour Community High School, where she earned her high school diploma. Her education provided her with a solid foundation in research methodologies and health sciences.
Certification and Expertise
Jessica is a Certified Clinical Research Professional (CCRP), a certification that underscores her proficiency and dedication to the field of clinical research. Her expertise extends to managing oncology clinical trials, designing and analyzing research studies leading to publications, and ensuring compliance with FDA/ICH-GCP guidelines. Additionally, she has a substantial background in teaching and mentoring individuals in clinical trials and health sciences.