Catherine D’Arcy is the Associate Director of Operations for Vivli. Prior to joining Vivli, Catherine gained 30 years of experience in the pharmaceutical industry, most recently managing data sharing requests for GlaxoSmithKline, and prior to that within clinical trial operations. She has a bachelor degree in Medical Biochemistry from the University of London.
Category: Staff
Liz Graham
Liz Graham serves as Senior Clinical Research Data Manager for Vivli. She received a Master of Public Health (MPH) from the University of New England and a Master of Data Science and Analytics (MS) from the University of Maryland. Additionally, she completed the Cross Cultural Health Immersion to Ghana, West Africa as part of a multidisciplinary team that evaluated integration of western health approaches with local medicine to improve cultural competence awareness.
Prior to this role, Liz coordinated multi-disease clinical trials at Johns Hopkins. She developed experience in oncological trial management, clinical EDCs, regulatory and protocol compliance standards. Liz is a member of the American Public Health Association and American Health Information Management Association.
Amrutha Baskaran
Amrutha Baskaran serves as the Product Director at Vivli. She received a MD from Tbilisi State Medical University, Republic of Georgia and a master’s degree in Clinical Research from the Medical University of South Carolina (MUSC). In addition, she completed a Fellowship in Clinical Research Ethics from the South Carolina Clinical and Translational Institute at MUSC.
Prior to the current position Amrutha worked as a Clinical Trial Lead for a medical device company running clinical trials on aortic stent grafts. She has 6 years of clinical trials experience in both academia and industry setting. She has experience in various roles as the study lead, data manager and regulatory specialist which gave her the exposure of working on both national and global clinical trials. In the past, Amrutha served as an Institutional Review Board member at the University of California, San Diego and as an external reviewer for Clinical Research Ethics Consultation Services at MUSC.