Amanda Vandike
About Amanda Vandike
Global Trial Manager at Bristol Myers Squibb
Amanda Vandike currently holds the position of Global Trial Manager at Bristol Myers Squibb. In this role, she manages global insourced and outsourced interventional clinical trials, guiding them from concept to final clinical study report. She provides quality oversight of CRO and vendors, ensuring compliance with ICH GCP, Regulatory Authorities regulations/guidelines, and SOPs/WPs. She also focuses on project management, supporting the management of issues, risks, timelines, and budget in clinical trials while acting as the primary operational contact for studies. Additionally, she leads cross-functional global teams for study execution.
Experience at IQVIA
Amanda Vandike previously worked at IQVIA in a variety of roles. From 2021 for six months, she was a Senior Clinical Lead. Prior to this, she served as Clinical Lead from 2019 to 2021 for two years, and as Associate Clinical Lead from 2018 to 2019 in the Cincinnati Area, KY. She initially joined IQVIA as a Senior Clinical Research Associate 2, Country Champion, and served from 2016 to 2018 in the Cincinnati Metropolitan Area. During her tenure, she progressed through increasingly responsible positions, gaining extensive experience in clinical research and project management.
Education in Pharmacology and Toxicology
Amanda Vandike has a strong academic background in pharmacology and toxicology. She earned a Master of Science (M.S.) from Wright State University Boonshoft School of Medicine in 2016. This educational background has provided her with a deep understanding of pharmacology and toxicology, which has been integral to her roles in clinical trial management and research.
Bachelor's Degree in Neuroscience
Amanda Vandike completed her Bachelor of Science (B.S.) in Neuroscience at the University of Cincinnati in 2013. This solid foundation in neuroscience has equipped her with the knowledge and skills necessary for understanding complex clinical research data and effectively managing clinical trials. Her education in neuroscience has been a critical component of her professional development and success in the field.
Early Career and Diverse Roles
Before her extensive career in clinical research, Amanda Vandike worked at Medpace as a Clinical Research Associate III from 2013 to 2015 in Cincinnati Area, OH. Additionally, she served as a French Tutor at the University of Cincinnati from 2011 to 2013. These early career roles demonstrate her versatility and commitment to education, providing a strong foundation for her subsequent roles in clinical research and trial management.