Tilda Research provides AI-powered “teammates” that integrate with sponsor and CRO workflows to automate clinical trial operations, improving data quality and cutting study timelines by up to 70%. Their platform connects to existing tools, handling tasks such as monitoring, finance, coordination, project and data management, enabling faster, more efficient trial execution.
Funding
Funding not disclosed
Founders
Product
Problem
Clinical trial operations often rely on manual processes, fragmented tools, and extensive paperwork, leading to slow study timelines, data entry errors, and challenges in maintaining regulatory compliance.
Solution
Tilda Research offers AI‑powered “teammates” that embed within sponsor and CRO workflows, automating routine tasks across monitoring, finance, coordination, project management, data handling, and investigator support. By leveraging machine‑learning‑driven automation, the platform reduces study timelines by up to 70% while enhancing data quality and ensuring continuous regulatory adherence. The solution operates within existing software ecosystems, providing real‑time visibility and predictive insights without requiring major workflow changes.
Target Audience
Primary customers are pharmaceutical sponsors and contract research organizations (CROs) seeking to accelerate trial execution, as well as research sites that need to reduce operational burden and improve data accuracy.
Features
- AI‑driven monitoring assistant that provides secure, live data dashboards for trial oversight
- Automated financial management, including payment tracking, revenue prediction, and intelligent follow‑up
- Coordinated project‑management teammate that streamlines task assignment, site activation, and protocol compliance
- Data‑management AI that eliminates double entry, enforces endpoint consistency, and updates documents in real time
- Investigator support module that guides protocol adherence and streamlines patient enrollment
- Built‑in regulatory compliance engine aligned with international guidelines for inspection readiness
- Seamless integration with sponsors’ and CROs’ existing tools and systems via APIs
- Real‑time centralized monitoring and reporting for faster decision making