Tundra Space

Tundra Space

Win More Trials. Grow Your Site.

The directory where research sites get discovered — by sponsors, CROs, and the AI tools they use. Structured profiles, AI-powered trial matching, and a full clinical research platform.

SiteSiteSiteTundraSponsorCROSponsor

How It Works

From signup to your next trial in three simple steps.

1

Create Your Profile

Build an AI-optimized profile with your PI, therapeutic areas, equipment, and patient population — discoverable by search engines and AI tools.

2

Get Matched

Our AI curates a personalized feed of trials from sponsors and CROs that fit your site.

3

Win Trials

Prove feasibility with real patient data, connect with sponsors, and land contracts.

1

Create Your Profile

Build an AI-optimized profile with your PI, therapeutic areas, equipment, and patient population — discoverable by search engines and AI tools.

2

Get Matched

Our AI curates a personalized feed of trials from sponsors and CROs that fit your site.

3

Win Trials

Prove feasibility with real patient data, connect with sponsors, and land contracts.

Everything Your Site Needs

From getting discovered to managing trials, all in one platform.

Site Directory

List your site in an AI-optimized directory. Get discovered by sponsors, CROs, and the AI tools they rely on.

AI Trial Matching

A personalized feed of relevant trials based on your therapeutic areas, capabilities, and patient population.

EHR & Patient Feasibility

Connect your EHR or patient database to prove your patient population and feasibility with real data.

Community & Chatrooms

Join a network of research professionals. Share insights, find collaborators, and stay connected.

Your Personalized Trial Feed

Our AI analyzes your site profile and delivers trials ranked by how well they match your capabilities.

AI-Matched Trials

Based on your site profile

4 new matches

Phase III Diabetes Management Study

NovaMed Therapeutics

Endocrinology
Phase III
120 needed
94% Match

Oncology Immunotherapy Trial

Apex Biosciences

Oncology
Phase II
80 needed
87% Match

Cardiovascular Risk Reduction

CardioVita Research

Cardiology
Phase III
200 needed
82% Match

COPD Inhaler Efficacy Study

BreathWell Pharma

Pulmonology
Phase II
150 needed
76% Match

Showcase Your Site

Build a comprehensive profile that helps sponsors find exactly what they need.

Lead PI & Credentials

Therapeutic Areas

Equipment & Facilities

Past Studies & Experience

Patient Population

Location & Catchment Area

AI-Optimized

The Site Directory Built for AI

Every profile is structured for AI crawlers and search engines. Sponsors and CROs find you whether they're browsing Google, asking ChatGPT, or querying Perplexity.

llms.txt

AI crawler instructions

Schema.org

Structured data markup

Public API

JSON endpoint for queries

XML Sitemap

Auto-generated for crawlers

NEW

Regulatory AI Assistant

Ask questions about FDA regulations, warning letters, and ICH guidelines. Get cited answers from real regulatory documents -- not hallucinations. Powered by 3,000+ FDA warning letters, 380+ CFR sections, and ICH guideline PDFs.

Regulatory AI

What are the AE reporting timelines under 21 CFR 312?

Under 21 CFR 312.32(c)(1), investigators must report serious and unexpected adverse events to the sponsor within 24 hours of first learning of the event.

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The Full Platform

Beyond trial matching, manage every aspect of clinical research in one place.

HIPAA Compliant

21 CFR Part 11

End-to-End Encryption

Don't Let the Next Trial Pass You By

Research sites on Tundra Space get found by sponsors, CROs, and AI tools — match to trials faster, prove feasibility with real data, and never miss an opportunity.

Questions? Contact us at research@tundraspace.com