Clinbook is a clinical trial intelligence platform that uses AI to provide sponsors, CROs, and research sites with data-driven insights for study planning, site selection, and investigator matching. By aggregating user‑generated data such as verified community reviews, site‑reported capabilities, and operational details, it helps sponsors activate high‑performing sites faster and enables investigators to be discovered by relevant trial opportunities.
Funding
Funding not disclosed
Founders
Product
Problem
Clinical trial sponsors and CROs often lack comprehensive, unbiased data on site performance and investigator expertise, making study planning and site selection inefficient and prone to enrollment delays. Existing information sources are fragmented, outdated, or biased, limiting the ability to identify diverse, high‑performing sites quickly.
Solution
Clinbook offers an AI‑driven clinical trial intelligence platform that aggregates verified, user‑generated data—including community reviews, site‑reported capabilities, and investigator‑reported credentials—to create a unified, searchable knowledge base. The system applies machine‑learning models to rank and match sites and investigators based on performance, therapeutic expertise, and patient population fit, enabling sponsors and CROs to plan studies and select sites with greater confidence. Investigators and research sites can maintain and showcase detailed profiles, increasing visibility to relevant trial opportunities. By centralizing real‑world feedback from verified clinical professionals, Clinbook reduces reliance on anecdotal information and accelerates enrollment timelines, helping therapies reach market faster.
Target Audience
Primary customers are pharmaceutical sponsors, contract research organizations, and research sites seeking data‑driven site selection, as well as investigators looking to increase visibility for trial participation.
Features
- AI‑powered search and ranking engine that surfaces high‑performing, diverse sites and investigators based on multiple data dimensions
- Verified community reviews from sponsors, CROs, site coordinators, CRAs, and CTMs providing candid, unbiased feedback
- Direct site‑reported capability data covering infrastructure, therapeutic expertise, and operational capacity
- Investigator‑reported credentials including trial history, publications, and patient population specialties
- Integrated profile management tools allowing sites and investigators to update capabilities and attract suitable trial opportunities
- Dashboard visualizations for enrollment forecasting, diversity metrics, and performance benchmarking
- Secure aggregation of both public and private data sources with role‑based access controls