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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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IQVIA at SCOPE Summit 2025: Day 1 Recap
Feb 11, 2025
Today, we kicked off the 2025 SCOPE Summit in Orlando, FL., and the IQVIA team is thrilled to join industry leaders, researchers and innovators to explore the latest advances in clinical operations and research.
Before the official start of SCOPE, we hosted an IQVIA Technologies Innovation Day. This pre-conference interactive event was designed to tackle the key challenges across the clinical trial lifecycle and how technology can improve the patient and site experience. Highlights included:
- Industry Panel: Panelists shared the challenges and advances in clinical trials from the perspective of the sponsor, site, and patient.
- Roundtable Challenge: Participants debated topics including digital adoption, operationalizing patient centricity, clinical trial finances and improving sponsor-site-CRO communication in focused roundtables.
- Networking & Demo: Attendees connected with industry peers, reviewed product demonstrations with technology experts and discussed the future of clinical operations to conclude the event.
This event marked the beginning of a week filled with several noteworthy sessions, networking opportunities, groundbreaking discussions and a chance to engage in thoughtful conversation with new and known industry colleagues.
The first official day of the conference was filled with several noteworthy sessions and hot topic discussions, including:
- Opening Plenary: The day started with an inspiring session titled “The Future of Clinical Trials,” in which experts discussed the evolving landscape of clinical research and the importance of patient-centric approaches.
- Clinical Data Strategy and Analytics Track: Melissa Mooney, director, eCOA Solutions Engineering, presented “Using eCOA Technology to Drive Endpoint Protection, Clinical Data Strategies, and Analytics.” She emphasized how eCOA solutions enhance data collection, management and review processes to ensure robust endpoint protection and improved clinical data strategies.
- Budgeting and Resources Track: Zahiah “Zee Zee” Gueddar, senior director and commercial lead, Financial Management Suite, led “End-to-End Financial Management: Challenges and Opportunities,” discussing how purpose-built SaaS and tech-enabled services can streamline budgeting and financial management to help reduce burdens on overloaded site staff and potential errors due to fragmented and manual processes.
- Booth and Demos: Throughout the day, our team at the IQVIA booth demonstrated our latest technologies and solutions. Attendees had the opportunity to interact with product experts, ask questions and see firsthand how our innovations can enhance clinical trial processes.
We have plenty of exciting sessions and presentations to look forward to this week at SCOPE. This week’s agenda includes:
- Wednesday, February 5, from 9:55 - 10:25 a.m. — Clinical Supply & Logistics Track: Cara Woodruff, director of Product Management, IT Design and Development at IQVIA Technologies, will present “Mitigating Risk and Complexity in Cell & Gene Therapy Trials with IRT.” This session will explore how to optimize pre-trial and pre-screening activities and reduce CAGT trial cost and risk with advanced drug supply chain IRT solutions.
- Wednesday, February 5, from 9:55 - 10:25 a.m. — Site Engagement & Enablement Track: A panel discussion titled “Helping Sites Succeed: An Industry-Wide Approach to Reduce Tech Burden” will feature Nick Whitney, senior director of Trial Management at IQVIA Technologies, along with other industry leaders. They will discuss strategies to reduce site tech overload and improve site efficiencies and study timelines.
- Thursday, February 6, from 8:25 - 9:10 a.m. — Patient-Centric Trial Design & Inclusive Research Track: Katie Shaw, senior director of Patient Recruitment & Enablement at IQVIA, will join a panel on “Actionable Strategies to Promote Diversity in Clinical Research Participation.” Panelists in this discussion will share examples of key efforts that have helped make progress toward broadening clinical research participation.
Stay tuned for more updates as we continue to explore the future of clinical operations at the SCOPE Summit 2025!