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Investigator Database

Identify and qualify clinical research sites globally from 300,000+ investigators and 100,000+ sites, with search filtering, historical data integration, and feasibility workflow automation.

Solution by Trial Interactive
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Overview

Trial Interactive's Investigator Database is a comprehensive clinical site and investigator discovery platform designed to help life sciences organizations expedite the path to site activation. By aggregating data from accredited public sources such as ClinicalTrials.gov, NIHR, and PubMed, the platform provides detailed records for over 300,000 investigators and 100,000 sites worldwide, enabling sponsors and CROs to identify, prequalify, and manage the best-fit sites for their clinical trials.

With over 50% of sites failing to successfully enroll patients, the Investigator Database is built to reduce that risk. The platform helps organizations save up to 25% on patient enrollment costs, avoid delays, and shorten site activation time by as much as 8 months by ensuring the right sites are selected from the outset.

Key Capabilities

  • Search an exhaustive collection of public data from sources including ClinicalTrials.gov, NIHR, and PubMed, covering detailed records for over 300,000 investigators and 100,000 sites globally.
  • Import historical investigator and site data to build a proprietary, tailored database aligned to your organization's specific research requirements.
  • Search and filter sites and investigators based on study-specific parameters including geographical location, therapeutic area, training, past clinical trial experience, and contact information.
  • Create and save collections of investigators and sites to support future site identification efforts and accelerate feasibility assessments.
  • Send data directly to TI eFeasibility to initiate site feasibility questionnaires (SFQs), and return response data back to the Investigator Database to continuously enhance site and investigator records for future studies.
  • Identify best-fit sites throughout the study start-up process to reduce the risk of site failure and protect enrollment investments.

Platform Highlights

  • Multilingual translation support to facilitate global site identification efforts.
  • 24/7 help desk available via email and phone support.
  • Reusable site and investigator collections to streamline repeated feasibility workflows.
  • Integration with the broader Trial Interactive ecosystem, including eTMF, Content Management, Trial Management, and Learning Management modules.

The Investigator Database integrates seamlessly within the Trial Interactive platform, enabling end-to-end clinical trial site management from initial identification through activation, while connecting with complementary tools such as eTMF services and trial management solutions.

Meta

Domain
Clinical Trial Management
Subdomain
Clinical Trial Management Systems (CTMS) & eTMF
Software type(s)
Database / Knowledge Base
Deployment type(s)
Cloud / SaaS
Industry vertical(s)
PharmaBiotechCRO
Development stage(s)
Clinical
Target user(s)
Research ScientistQA / Regulatory AffairsClinical / Diagnostic Professional
Compliance standard(s)
GxP