Adaoma Aigbodion
About Adaoma Aigbodion
Adaoma Aigbodion is a Sr. Clinical Trial Monitor at Bristol Myers Squibb and an instructor at Clinical Research Fastrack, with extensive experience in clinical trials and therapeutic areas such as Pain management, Cardiovascular, and Oncology.
Current Company
Adaoma Aigbodion currently works at Bristol Myers Squibb as a Sr. Clinical Trial Monitor. In this role, she is responsible for overseeing clinical trial operations, ensuring compliance with study protocols, and monitoring study sites. Her extensive experience in clinical research makes her a vital asset to the company.
Teaching Role
In addition to her primary role, Adaoma Aigbodion serves as an Instructor at Clinical Research Fastrack in the Greater Philadelphia Area. She educates aspiring clinical research professionals, leveraging her extensive industry knowledge to provide practical, real-world insights into clinical trial management and monitoring.
Past Experience
Adaoma Aigbodion has amassed significant experience working with various organizations in the clinical research field. She has served as Senior CRA II at Syneos Health from 2018 to 2020 and as Senior CRA at inVentiv Health Clinical from 2017 to 2018. Prior to these roles, she was a Clinical Research Associate II at PPD from 2015 to 2016, and a Clinical Research Associate I at ICON plc from 2013 to 2015, having started at ICON plc as a Study Start Up Associate from 2011 to 2013. Additionally, she spent four months as a CRM Fellow at the Partnership for Public Service in 2011.
Educational Background
Adaoma Aigbodion holds an MS in QA/RA-Clinical Trial Management/Drug Development from Temple University, achieved between 2012 and 2014. She also earned a BS in Biomedical Engineering from Rutgers University, where she studied from 2002 to 2007. Her educational background lays a strong foundation for her career in clinical research.
Areas of Expertise
Adaoma Aigbodion has extensive experience in various therapeutic areas, notably pain management. She has been involved in the implementation of study protocols for Phase 1-IV clinical trials and has expertise in the monitoring of study sites and on-site data management. Additionally, she has managed clinical trials in therapeutic areas such as Cardiovascular, Oncology, Musculoskeletal, Vaccines, and Neurology, and has a background in the collection of study-related documents.