From bottlenecks to breakthroughs: Human-centred strategies for faster study starts
Accelerate feasibility, startup and activation through site-centric, data-driven approaches
Clinical trial startup is increasingly complex. Sites face longer timelines, heavier burdens and persistent delays in contracting and budgeting. ICON’s recent industry survey of over 100 principal investigators and senior site professionals reveals these challenges and the need for smarter, more supportive approaches to site activation.
This whitepaper outlines the results from our industry survey and highlights the actionable strategies of how ICON is supporting sponsors to streamline start-up and empower clinical sites including:
- Implementing site engagement approaches that balance alignment and competing priorities
Utilising human-enabled predictive analytics to identify optimal sites and streamline budget and contract negotiations
- Adopting data-informed over-selection strategies to improve site readiness and reduce attrition
Accelerating contract and budget negotiations with SmartDraft AI, cutting cycle times and speeding activation
Building stronger site relationships through dedicated liaisons and embedded experts who drive momentum
Simplifying site training, documentation and communication with the FIRECREST portal for faster, tech-enabled startup
Whitepaper
From bottlenecks to breakthroughs: Human-centred strategies for faster study starts