Sarah is a Senior Clinical Research Manager at Vivli. She received a Bachelor of Science in Biomedical Science (BS) from Salem State University in 2015 and a Master of Science in Biotechnology, Bioinformatics (MS) from University of Maryland in 2022.
Prior to this role, Sarah has worked in a Molecular Biology laboratory as an Associate Scientist at Azenta Life Sciences. Most recently, she worked at a precision oncology company, Guardant Health, which specializes in liquid biopsy. Here, she served as a supervisor where she led Biospecimen management operation teams in the San Diego and Redwood City laboratories and gained experience in clinical trial sample management and clinical trial project coordination.
The NIH Data Management and Sharing (DMS) policy went into effect in January 2023 to promote the sharing of scientific data.
Please watch Vivli’s recent webinar and find out more about how Vivli can help you navigate the NIH Data Management and Sharing policy. Hear from academic staff on their experiences in supporting researchers with their Data Management and Sharing Plans (DMSP).
During this webinar, we:
- Provide an overview of Vivli, including what types of data should be shared in Vivli
- Discuss the benefits of using Vivli to meet the data sharing requirements of your NIH grant
- Review the steps to completing the NIH DMSP and budget justification
- Hear views from academic staff on their experiences supporting researchers to complete the new NIH DMSP
Speakers include:
- Anne Seymour, Johns Hopkins University
- Amy Nurnberger, Massachusetts Institute of Technology
- John Borghi, Stanford University
- Rebecca Li and Julie Wood, Vivli
Participants had the opportunity to ask questions. This webinar is most useful for current or prospective NIH grantees or those who support them.
Irene Troupansky is the Senior Software Architect at Vivli.
Prior to joining Vivli, Irene was a Senior Software Architect at Examity where she helped the company to launch its first Cloud SaaS Multi-Tenant version of Examity Platform and lead its further design and development through the company rapid growing, insuring Examity’s leading place as online proctoring provider. Prior to Examity, Irene was a Lead Architect/Developer at Tracker Systems, where she helped the company to upgrade its product to a Cloud SaaS version and lead the product further design and development.
William Gourgiotis is a Technical Operations Engineer at Vivli, focused on building and maintaining scalable, secure cloud-based research environments that support global data access and clinical research initiatives. He joined Vivli in 2021 and has a background in IT operations, cloud infrastructure, and enterprise technical support, including experience with the State of New Hampshire Department of Information Technology.
In his role, William supports the reliability and performance of cloud platforms, with a focus on automation to streamline operations, reduce manual overhead, and improve system efficiency. His work spans infrastructure operations, environment management, and technical support across cloud-based systems.
William holds a Bachelor of Science in Computer Science (UMass Lowell) and a Bachelor of Arts in Criminal Justice (Plymouth State University).
Catherine D’Arcy is a Principal at 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.
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 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.
