Stop losing eligible candidates in manual screening.
TrialBridge helps clinical research teams turn protocols, candidate records, visit windows, and follow-ups into one clear enrollment workflow.
Strong alignment with key inclusion criteria. Two items need coordinator review.
Missed prep · 2 reminders unread
“Patients on stable beta-blocker therapy ≥ 4 weeks are eligible.”
A single worklist sorted by what moves enrollment forward today — strong matches, missing data, visits to confirm, follow-ups due.
Every recommendation cites the protocol section it came from.
Visit windows and retention signals surface before they close.
One unified workflow.
Focus on what moves the study forward.
A single coordinator worklist, sorted by what needs you next.
- 7Strong matches
- 9Missing data
- 5Visits to confirm
- 3Follow-ups due
- Review new candidates10
- Eligibility reviews5
- Follow-up calls4
- Queries to resolve3
- Safety review1
Every candidate has a next step.
See where each candidate stands and what needs review next.
Criterion-by-criterion review.
Review matches, missing data, possible exclusions, and protocol evidence in one place.
Answers must show evidence.
Ask protocol questions and get cited answers with review-safe language.
Yes — the patient has not received prior systemic therapy, satisfying §5.2.4. Coordinator review required before locking eligibility.
Catch issues before visits are missed.
Track confirmations, prep tasks, reminders, and support signals.
- CAND-0234Missed eDiary · 2 daysMedium
- CAND-0157Travel distance · 1 dayMedium
- CAND-03813 reminders unreadHigh
- CAND-0773All on trackLow
Practical plans for research teams.
Start with one site or coordinate workflows across studies, locations, and approved reporting teams.
For one research site running active studies with a coordinator-led workflow.
- All modules: Brief, Pipeline, Eligibility, Copilot, Visits, Retention, Reports
- CSV imports and protocol uploads
- Coordinator, sub-I, PI, auditor roles
- Audit history on every action
- Email support
For multi-location teams that need shared templates, network visibility, and standard reporting.
- Everything in Single Site
- Multi-site pipeline & workload view
- Shared eligibility and reminder templates
- Network-level reports with site breakdown
- Onboarding support included
For approved summary-level viewers supporting sites without raw candidate access.
- Read-only viewer role · scoped per study
- Approved summary reports (CSV / PDF / JSON)
- Export history with actor and timestamp
- No raw candidate identifiers
- Configurable cadence
Pricing depends on active studies, site count, coordinator seats, and reporting needs.
Verified across an academic site network.
“The latency in getting a candidate flagged as ‘high risk’ was previously unacceptable. TrialBridge compresses that window from days to hours automatically. It moves beyond a database into an active operational tool.”
Source: Annual Operational Review Cycle 07; backend telemetry and customer feedback loops captured through 15 June 2026.
Built for careful research operations.
Capability-based controls. No black boxes, no hidden decisions.
Coordinators, sub-Is, and PIs see only what their role allows.
Every action and decision is captured in an append-only log.
Answers cite section, version, and a quotable source.
Outreach uses templates that pass coordinator review before send.
Candidate identifiers stay scoped to your site by default.
See TrialBridge on your workflow.
Start with your protocol, candidates, and coordinator priorities.