Tuesday December 3, 2024
3:00 pm – 3:45 pm
Breakout

Breakout Session II

Dive deeper into specific topics in these focused and interactive discussions.

2:45 pm – 3:45 pm
Sala XIV/XV
Breakout

Building Tomorrow: Team Structures For Success & Growth

Learn how to optimize your team structure to encourage success and future growth. Explore strategies for cultivating cohesive and dynamic teams, enhancing communication, and aligning roles and responsibilities to maximize efficiency in clinical research.

2:45 pm – 3:45 pm
Sala VI
Breakout

Collective Action: Attracting More Clinical Studies To Europe

European research sites are poised to attract even more studies with the right resources. Learn how to leverage regional strengths to bolster Europe’s position as a premier destination for clinical research. Discover strategies for navigating cross-border regulatory processes and showcase your site’s capabilities.

2:45 pm – 3:45 pm
Sala XII
Breakout

Facilitating Patient Access In Cross-Border Clinical Research

Explore strategies and best practices for facilitating trial participant access across borders. This session will provide practical insights into overcoming regulatory, logistical, and cultural barriers to ensure seamless participation and collaboration.

2:45 pm – 3:45 pm
Sala VII
Breakout

From Diversity Action Plans To Inclusive Enrollment: Strategies For Success

This session will provide strategies for European clinical research sites to actively contribute to and align with sponsor DEI goals. We will explore practical approaches for your site’s DEI plan, ensuring inclusive patient enrollment and retention. Learn how effective collaboration between sponsors and sites can drive equitable research outcomes and position European sites as leaders in diversity equity and inclusion.

2:45 pm – 3:45 pm
Sala XIII
Breakout

Streamlined Success In Study Start-Up

This session will share practical methods to optimize the clinical research study start-up process. Uncover proven methods to streamline protocol development, enhance regulatory compliance, expedite site selection, and improve study initiation efficiency. Join us to discuss best practices for achieving faster study start-up and smoother clinical trial execution.