Tina Tran
About Tina Tran
Tina Tran is a Sr. Clinical Trial Associate at Bristol Myers Squibb with over 8 years of experience in clinical research and trial management.
Current Role at Bristol Myers Squibb
Tina Tran is currently a Senior Clinical Trial Associate at Bristol Myers Squibb. She joined the company in November 2019. Her role involves managing and overseeing multiple aspects of clinical trials, contributing significantly to the development and implementation of various clinical studies. With over eight years of experience in clinical research and trial management, she brings a wealth of knowledge and skills to her position at Bristol Myers Squibb.
Previous Experience at Celgene
Before joining Bristol Myers Squibb, Tina Tran worked as a Senior Clinical Trial Associate at Celgene in San Diego, California. Her tenure at Celgene lasted from 2018 to 2019, during which she contributed to several clinical trials. Her work at Celgene was pivotal in advancing new therapies, leveraging her comprehensive experience in trial management and clinical research.
Clinical Project Assistant at PPD
From 2015 to 2018, Tina Tran served as a Clinical Project Assistant II at PPD. Over her three years at PPD, she acquired significant experience in clinical project assistance. This role enabled her to gain a deeper understanding of clinical trial processes and procedures, further solidifying her expertise in the field.
Front Office Specialist at Planned Parenthood
Tina Tran also has experience in healthcare operations, having worked as a Front Office Specialist at Planned Parenthood of the Pacific Southwest from 2014 to 2015. In this role, she managed front office tasks and supported healthcare services, which provided her with valuable insights into patient management and healthcare administration.
Education and Public Health Background
Tina Tran holds a Bachelor of Science (BS) in Public Health from San Diego State University-California State University. Her strong background in public health provides a solid foundation for her clinical research roles. She effectively leverages her academic knowledge to enhance her contributions to clinical trials and healthcare initiatives.