Born from the collective insights of the Research Revolution community, the Site Enablement Model addresses the evolving challenges in clinical research. It goes beyond adopting new technologies; it’s about reimagining how trial sponsors and Clinical Research Organizations (CROs) collaborate and support research sites.

By fusing modern technology with streamlined operations and data analytics, we’re setting the stage for a new era in clinical research.

Step 1:

Where does your organization stand in this revolution? The Site Enablement Maturity Assessment is your roadmap to understanding your current position and pinpointing areas of growth. 

Step 2:

This comprehensive guide breaks down the five core site enablement capabilities, providing actionable steps to enhance your site enablement maturity, leading to efficient operations, improved data quality, and better patient outcomes.

Step 3:

Florence’s Site Enablement Platform offers tangible solutions to modern challenges. Connect with us to see how we can enhance your clinical research operations and why sites love working with our platform, ranking us #1 out of 191 platforms three years in a row.

Efficient clinical trial operations rely on automation and capacity management. This includes integrating with sites, real-time monitoring, automating tasks, and providing technology. Advancing in these areas boosts efficiency, reduces errors, and improves data exchange, enhancing site trial capacity.

Remote collaboration is crucial in the modern digital landscape. It assesses your organization’s remote monitoring, data handling, document sharing, training, and tech approach. Advancements enhance data quality, speed up issue resolution, and enable a flexible trial site approach.

Building relationships with study sites is crucial for successful clinical trials. This aspect assesses your organization’s dedication to training, communication, and support. Strengthening engagement practices enhances enrollment, protocol adherence, data quality, and fosters site relationships.

Effective clinical trial oversight requires managing site operations and reporting. This includes site selection, data collection, analysis, operational decision-making, and inspection readiness. Maturing in this area leads to improved insights, decision-making, and risk reduction.

Your organizational design significantly impacts clinical trial outcomes. This encompasses site-centric dialogues, tech budgeting, and staffing for site technology enablement. Progressing in this area improves communication, resource utilization, and fosters a supportive environment for study sites.