Medidata at DIA 2022

Join Medidata
At DIA 2022

Join us for our speaking sessions and visit us at booth 1631

Our Presence

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 Staley
VP, Patient Engagement

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 Tucker
Managing Partner, Patient Cloud

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
Senior Director, Product Management

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.

Holly Robertson
Senior Director, Advisory Services
Shelley Douros
Senior Director, Product Management

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
Director, RTSM Customer Adoption

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.

Nadia Bracken
Operational Advisor, RBQM

Nadia Bracken is an Operational Advisor with a background in clinical trial management consulting. At Medidata, she is focused on support for Risk Based Quality Management (RBQM) products, client services, and process oversight. Nadia has 15+ years of prior Clinical Operations experience across multiple therapeutic areas at small specialty biotechs, CROs, and industry-leading pharmaceutical companies. As a clinical researcher networking facilitator, she regularly hosts virtual and in-person educational, professional development forums, and social events. Nadia speaks and leads workshops/round-tables at global drug development conferences. She is a champion for working more effectively to advance important clinical developments and patient-centric operations for clinical trials.

Visit us at Booth #1631