Medidata at DIA 2022
Join Medidata
At DIA 2022
Join us for our speaking sessions and visit us at booth 1631
Our Presence
- Pre-Event, Tuesday June 16th
- Day 1, Monday June 20th
- Day 2, Tuesday June 21st
- Day 3, Wednesday June 22nd
Join us at these sessions, across three days of the program, to learn about how we are solving key challenges in clinical operations.
| Time | Title | Track/Subtrack | Speaker(s) |
| 2:00 – 5:00 PM CT | Become a DCT Master: Understanding the Lifecycle of Decentralized Clinical Trials | Pre-Event: Virtual Short Course | Brian Barnes, Senior Director, Product Management
Holly Robertson, Director, Advisory Services Michael Tucker, Managing Partner, Patient Cloud |
Join us at these sessions, across three days of the program, to learn about how we are solving key challenges in clinical operations.
| Time | Title | Track/Subtrack | Speaker(s) |
| 1:15 PM CT | Adaptive Designs Save Time & Money: Regulatory Agencies Accept Them – Why Aren’t They Used More? | Clinical Trials and Clinical Operations | Marc Kaufman, Director, RTSM Customer Adoption and Value Realization |
| 1:15 PM CT | Risk-Based Monitoring in Clinical Trials: An Evolution of Practices During the COVID Pandemic | Clinical Trials and Clinical Operations, R&D Quality and Compliance | Brian Barnes, Senior Director, Product Management |
| 4:00 PM CT | Design Thinking: The Empathy Map | Professional Development | Nadia Bracken, Operational Advisor, RBQM |
Join us at these sessions, across three days of the program, to learn about how we are solving key challenges in clinical operations.
| Time | Title | Track/Subtrack | Speaker(s) |
| 11:15 AM CT | Preparing for the Future of Research and Development: 10-Years of Multistakeholder Innovation, Collaboration, and Transformation | DIAMond Sessions | Jackie Kent, EVP Chief Customer Officer |
Join us at these sessions, across three days of the program, to learn about how we are solving key challenges in clinical operations.
| Time | Title | Track/Subtrack | Speaker(s) |
| 9:00 AM CT | Transformation of the Data Manager to the Data Scientist | Data and Technology in Clinical Trials | Shelley Douros, Senior Director, Product Management |
| 4:15 PM CT | Collaboration to Improve Definitions, Nomenclature, KPIs, and Readiness Frameworks for the Adoption of Decentralized Research | Clinical Trials and Clinical Operations
Data and Technology in Clinical Trials |
Alicia Staley, Vice President, Patient Engagement |
Meet Our Experts
Our industry experts are available and excited to meet with you to discuss your business challenges and the opportunities to work together.
Our Onsite Team
Alicia has over 20 years of experience in software design and information systems management. She has a Mechanical Engineering Degree from Syracuse University and from Boston University with a Masters of Information Systems and an MBA.
At Medidata, Alicia works to infuse the patient perspective throughout the product development lifecycle and help engage patients in novel ways. Alicia is also a three-time cancer survivor, first diagnosed with Hodgkin’s disease as a sophomore during college.
Over the past 10 years, she's applied her engineering background to improve the patient experience for those dealing with cancer. With an extensive network of patient advocates and non-profit organizations, she collaborates with a wide range of stakeholders to help improve processes and policies that impact cancer care.
Michael is a member of Medidata’s Mobile Health team and is a subject matter expert in electronic informed consent and virtual trials. Over the last six years, Michael has worked collaboratively with sponsors, CROs, regulators, ethics committees and researchers around the world to pioneer the use of electronic informed consent and virtual trials. His 30-year career in medical research includes eight years with the US government conducting and supporting surgical research and 22 years working in the commercial sector to provide technology solutions that improve and support preclinical and clinical research. Michael has been a participant in two clinical trials...but had to consent on paper because eConsent had not been invented yet! Michael is a decorated veteran of the United States Navy and resides in Austin, Texas where he is also an elected public official serving his local community.
Brian Barnes is a Senior Director, Product Management – RBQM for Medidata Solutions. Brian has 16 years in clinical development and has specifically supported RBQM for ten years specializing in operational solutions for small to large pharma, biopharma, and biotech companies. Brian is a co-liaison within the Association of Clinical Research Organizations (ACRO) RBQM Working Group and presented and published on the topic of RBQM at industry meetings, conferences, and journals.
Shelley Douros is Senior Director of Product at Medidata, a Dassault Systèmes company, focusing on clinical trial planning and budgeting. She has over 20 years of experience dedicated to cross-functional collaborations specific to clinical trial budgeting and forecasting, business operations, outsourcing, and investigator budget development and negotiations. Shelley has spearheaded the creation of financial lifecycle platforms for both sites and sponsors. She has served as a speaker and chair at numerous industry conferences and has authored many published articles. Shelley has a passion for uncovering pain points and identifying strategic solutions that lead to faster, effective, and mindful patient care.
Marc Kaufman has been in the Life Sciences Industry for close to 20 years, specializing in IRT/RTSM technology for the past 15 years.
Marc is a Director-RTSM Customer Adoption and Value Realization at Medidata Solutions.
Marc has been at Medidata for 4 1/2 years and Marc is a thought leader on clinical trials with expertise on supply management strategies and decentralized trials.