Back To Schedule
Tuesday, June 26 • 1:30pm - 2:00pm
#250: Developing Standards to Support the Use of Wearables and Sensors for Objective Data Collection During Clinical Trials

Sign up or log in to save this to your schedule, view media, leave feedback and see who's attending!

Component Type: Session
Level: Intermediate
CE: IACET 0.50

Seating is limited.
The DIA Study Endpoints Community has convened a working group to drive the science around the use of wearable technology and the development of study endpoints from wearables data. Broad adoption of wearables and sensors for objective data capture in pivotal studies is being impeded by the absence of standards. In this discussion, participants will evaluate and provide feedback on proposed solutions intended to address this challenge.

Learning Objectives

Review and discuss the current work of Study Endpoint Community’s Wearables Work Group, and the Standards Work Stream; Evaluate the the adoption of wearables and sensors for objective data capture in clinical trials.


Jennifer C Goldsack


Susan Marie Vallow

Marie McCarthy

Paul O'Donohoe, MS

avatar for Jennifer Goldsack

Jennifer Goldsack

Senior Project Manager, CTTI
Jen Goldsack is a Senior Project Manager at the Clinical Trials Transformation Initiative (CTTI). Jen leads two projects within CTTI's Mobile in Clinical Trials (MCT) Program; the MCT Novel Endpoints, and MCT Mobile Devices projects.

Marie McCarthy

Senior Director of Product Innovation, ICON plc
Marie Mc Carthy, Senior Director of Product Innovation, is part of the multidisciplinary Innovation Team at ICON PLC. Her previous role was that of EU Sales and Marketing Manager with Philips Respironics, building awareness of the value of Actigraphy endpoints among Clinicians and... Read More →
avatar for Paul O'Donohoe

Paul O'Donohoe

Senior Director, eCOA Product and Science, Medidata Solutions, United States
Paul O’Donohoe is Senior Director, eCOA Product and Science at Medidata Solutions, a clinical software platform provider. He is responsible for providing strategic oversight of the development of Medidata's electronic clinical outcome assessment technologies, and supporting internal... Read More →
avatar for Susan Vallow

Susan Vallow

Executive Director, Patient-Centered Outcomes Research, Worldwide Clinical Trials
Susan Vallow, VP, Patient Centered Outcomes Strategy, MedAvante-ProPhase, is an experienced outcomes researcher with a specialty in the strategy, development and implementation of PROs. Sue previously was Senior Director & Head, Patient Focused Outcomes at GSK, where she managed the... Read More →

Tuesday June 26, 2018 1:30pm - 2:00pm EDT
Content Hub NE Lobby Boston Convention and Exhibition Center 415 Summer Street, Boston, MA 02210 USA