SCRS Talks

Join Amy Franco, Senior Director of Patient Liaisons at Scout [https://www.scoutclinical.com/], to explore how prioritizing patient satisfaction can lead to improved clinical trial outcomes. Amy shares Scout’s unique approach to easing the burden on both patients and sites through personalized travel coordination, reimbursements, and around-the-clock support.  She highlights how arranging transportation or reimbursing for childcare can make trials more accessible and reduce dropout rates. The conversation also dives into how Scout’s global patient liaison team and portal technology streamline administrative tasks for sites. Tune in to learn how a patient- and site-centric approach can transform trial success.

Veeva [https://www.veeva.com/]'s VP of Strategy, Bree Burks, reveals the strategic vision behind their groundbreaking free CTMS platform—a bold move designed to democratize technology access for clinical research sites of all sizes. Discover why Veeva prioritizes site success through standardization and simplicity, and how selecting the right technology partnerships can empower sites to scale operations and thrive.

Early investment in proper training doesn't just benefit new staff—it strengthens your entire organization and the research ecosystem. SCRS is ready to tackle industry-wide training gaps, transforming research assistants, coordinators, and business teams into confident contributors. Learn how this foundational knowledge accelerates success and helps your team navigate challenges with clarity and purpose. Save your seat today for the hands-on "Back to Basics" workshop at the Global Site Solutions Summit [https://sitesolutionssummit.com/event/global/registration/]this September in Orlando. This intensive training equips research newcomers with must-have skills to thrive in clinical trials.

Sit down with Rick Ward, Chief Commercial Officer at CRIO, to discuss the emerging concept of central eSource in clinical research. Rick explains how this model, which builds on the traditional eSource framework, can enhance standardization, streamline data collection, and reduce the burden of manual transcription. The conversation highlights the importance of site-driven technology, the flexibility required for real-world implementation, and the need for strong support infrastructure. Explore how CRIO’s approach is reshaping source documentation and creating new opportunities for both sites and sponsors.

Clinical research in Europe presents unique challenges, from navigating country-specific regulations to addressing language barriers and patient travel logistics. Scout [https://www.scoutclinical.com/]’s Moisha Platto and Courtney Dodge share how tailored solutions are enhancing clinical trial efficiency across Europe and what this means for sites, sponsors, and patients. Hear strategies for improving patient engagement, streamlining reimbursements, and ensuring compliance with regional regulations.