Jessica Garzon, Pharm D, R Ph
About Jessica Garzon, Pharm D, R Ph
Jessica Garzon, Pharm.D., R.Ph, is a Senior Clinical Scientist at Bristol Myers Squibb in Summit, New Jersey, with extensive experience in clinical research and development.
Current Title and Workplace
Jessica Garzon is currently a Senior Clinical Scientist at Bristol Myers Squibb. She operates out of Summit, New Jersey, United States. In this role, she brings her extensive expertise in clinical development to the forefront, contributing to the progress of important medical research and advancements.
Previous Experience at Celgene
Jessica Garzon held multiple roles at Celgene over the years. From 2019 to 2020, she worked as a Clinical Research Scientist for 7 months. Prior to that, from 2018 to 2019, she served as a Senior Associate Clinical Research Scientist for a year in Summit, New Jersey. Additionally, in 2015, she was a Pharmacy Extern for a month in Basking Ridge, NJ. During her tenure at Celgene, Jessica gained significant experience in early and late-phase hematology/oncology clinical development.
Work at Roche and Rutgers University
From 2016 to 2018, Jessica Garzon worked as a Post-doctoral Fellow in Clinical Science at Roche in the Greater New York City Area. Concurrently, she served as Adjunct Faculty at Rutgers University in Piscataway, New Jersey. These roles allowed her to deepen her expertise in clinical science and contribute to the academic community through teaching and mentorship.
Educational Background
Jessica Garzon completed her education at Rutgers University, where she graduated Magna Cum Laude and achieved a Doctor of Pharmacy (Pharm.D.) degree. Her academic journey spanned from 2010 to 2016. This rigorous educational background laid the foundation for her successful career in clinical science and pharmaceutical research.
Specialized Skills and Expertise
Jessica Garzon has expertise in early Phase 2 clinical development in neuroscience. She also has significant experience in early and late-phase clinical development in hematology and oncology. Her skill set includes proficiency in protocol and clinical document development, medical data review, and cross-functional communication. Additionally, she is knowledgeable about regulatory procedures within the pharmaceutical industry.