SCRS Talks

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.

SCRS’s Karri Venn takes a deep dive into the current state of clinical research coordinator salaries with Stacie Merritt, Director at Ascension St. John Clinical Research Institute. We analyze compensation trends, including salary ranges and bonuses, and how organizations can remain competitive in a rapidly evolving job market. Learn how sites of all sizes and types are compensating their workforce and the key factors influencing coordinator pay. Don’t miss this essential conversation packed with data-driven insights to help your site refine its compensation strategy, improve staff retention, and stay ahead in a competitive workforce landscape.

Clinical trials must represent the communities they serve—and the SCRS IncluDE Program [https://myscrs.org/include/] is equipping research sites to make that a reality. In this episode, SCRS' Kathy Mickel sits down with Kim Ribeiro, IncluDE Program co-chair, to discuss how sites and industry partners can make trials more accessible to all communities. We tackle the importance of staying focused on the science, cutting through the noise, and having real conversations about what’s working (and what’s not). Tune in to hear why the IncluDE Site Solutions Summit [https://sitesolutionssummit.com/event/include] is a must-attend event for sites, sponsors, and solution providers—and how you can be part of the collective shaping the future of representative research.

Megan Gross, Associate Director of Clinical Site Services at AiCure, shares how innovative strategies and AI-driven solutions are shaping the future of patient-centric clinical research. We explore common barriers to medication compliance, the role of trust and engagement, and how AI-powered technology can enhance adherence. Hear practical interventions that sites can implement to support participant adherence, engagement and retention.

David Vulcano, SCRS Honorary President, breaks down the recent ICH GCP R6 E3 revisions and explores their practical impact on clinical research sites. He discusses key topics such as the decentralization of trials, updated record retention guidelines, and the rising importance of digital health technologies and cybersecurity. David highlights that, although there’s considerable hype and some uncertainties, the new guidelines generally codify existing practices rather than overhaul them. The episode serves as a practical guide for sites to align their operations with both local regulatory requirements and the updated GCP standards while maintaining an open dialogue with sponsors and CROs.