Current Role at Stanford
In my role as Deputy Chief Information Officer, I provide strategic leadership and management of innovative technology solutions for Stanford Health Care and School of Medicine, as part of Stanford Medicine's Technology and Digital Solutions organization, led by Eric Yablonka. I provide direct oversight for functional areas in Research Technology, Data and Analytics, Educational Technology, Application Development and Research Informatics.
In my role as Associate Dean, Industry Relations and Digital Health, I lead Stanford Medicine’s Office of Industry Relations and Digital Health (IRDH) whose mission is to foster relationships that will promote discovery, accelerate the use of technologies that advance human health, and translate today’s breakthroughs into tomorrow’s standard of care. IRDH serves as the front door for organizations interested in exploring a strategic relationship with Stanford Medicine. The work is part of Stanford Medicine's Strategy Team, led by Priya Singh.
Honors & Awards
Amy J. Blue Award, Stanford University (2007)
Education & Certifications
BA, Stanford University, Human Biology, Honors in Neuro (1993)
Piano, music composition, painting, distance running, good restaurants, absolutely anything in Hawaii.
Professional Affiliations and Activities
Chair, Research IT Faculty Advisory Committee (2016 - Present)
Co-Chair, Clinical Research Informatics Task Force (2014 - Present)
Member, Stanford Medicine Genomics Executive Committee (2015 - Present)
Member, CIO Council, Stanford University (2011 - Present)
Member, SOM Administrative Steering Committee (ASC) (2009 - Present)
Member, MedEd Leadership Group (2011 - Present)
Member, Campus Strategic Technology Partners (2010 - Present)
Member, National Research Networking Working Group (CTSA-Based) (2009 - Present)
Chair, IRT Exective Committee (2009 - Present)
Member, Medicine X Advisory Board (2011 - Present)
Ten principles for data sharing and commercialization.
Journal of the American Medical Informatics Association : JAMIA
Digital medical records have enabled us to employ clinical data in many new and innovative ways. However, these advances have brought with them a complex set of demands for healthcare institutions regarding data sharing with topics such as data ownership, the loss of privacy, and the protection of the intellectual property. The lack of clear guidance from government entities often creates conflicting messages about data policy, leaving institutions to develop guidelines themselves. Through discussions with multiple stakeholders at various institutions, we have generated a set of guidelines with 10 key principles to guide the responsible and appropriate use and sharing of clinical data for the purposes of care and discovery. Industry, universities, and healthcare institutions can build upon these guidelines toward creating a responsible, ethical, and practical response to data sharing.
View details for DOI 10.1093/jamia/ocaa260
View details for PubMedID 33186458
Direct2Experts: a pilot national network to demonstrate interoperability among research-networking platforms
JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION
2011; 18: I157-I160
Research-networking tools use data-mining and social networking to enable expertise discovery, matchmaking and collaboration, which are important facets of team science and translational research. Several commercial and academic platforms have been built, and many institutions have deployed these products to help their investigators find local collaborators. Recent studies, though, have shown the growing importance of multiuniversity teams in science. Unfortunately, the lack of a standard data-exchange model and resistance of universities to share information about their faculty have presented barriers to forming an institutionally supported national network. This case report describes an initiative, which, in only 6 months, achieved interoperability among seven major research-networking products at 28 universities by taking an approach that focused on addressing institutional concerns and encouraging their participation. With this necessary groundwork in place, the second phase of this effort can begin, which will expand the network's functionality and focus on the end users.
View details for DOI 10.1136/amiajnl-2011-000200
View details for Web of Science ID 000299871300025
View details for PubMedID 22037890
View details for PubMedCentralID PMC3241163