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TrialMind for Research Institutions

Run studies without writing code

Investigators define patient cohorts and run analyses in plain language, on your institution's data and inside your environment.

Needed from the investigator
No code1
Needed from the investigator
Academic medical centers in production
21
Academic medical centers in production
Patient records moved out of your environment
Zero2
Patient records moved out of your environment

Academic research workflows

Five workflows. Each runs on your data, under your institutional review board (IRB) approval, with an audit trail.

TrialMind building an attrition table for a metastatic NSCLC cohort from a plain-language request
Attrition table for HER2-altered metastatic non-small cell lung cancer
When it is used
A principal investigator (PI) wants to know whether a study is possible before writing the protocol.
What it produces
Patient counts and the attrition table, defined in plain language.

Two academic medical centers

No code

Needed from the investigator

Clinical researchers query institutional data in plain language. TrialMind drafts an analysis plan for them to review, then runs it in the institution's secure environment, with no setup by the investigator.

  • Institutional data queried in plain language
  • An analysis plan reviewed before anything runs
  • No setup for investigators once the data is connected

Customer name available under a non-disclosure agreement (NDA).

Data security and IRB requirements

SOC 2 Type I & IIISO 27001HIPAA · BAAsGxP qualified

Runs inside your environment

Raw patient records do not leave it, which simplifies protected health information (PHI) governance and IT security review.

Business associate agreement (BAA) at onboarding

Signed alongside any data use agreement your privacy office requires.

Works under your IRB approval

TrialMind does not change your protocol. Every cohort and analysis step is reproducible.

Security and compliance details ›

Technical details

Data in
Observational Medical Outcomes Partnership (OMOP) data, i2b2, REDCap, electronic health record (EHR) extracts, published literature, and trial registries
Users
PIs, fellows, graduate students, and study staff; no coding required
Deployment
Inside your institution's environment; connects to your warehouse rather than moving data
Licensing tiers

Research Group

A single PI's lab or research group

  • Seats pooled across the PI, study staff, and trainees
  • Your institutional data sources connected
  • Onboarding for the group
  • Email support

Department

A department or division

  • Everything in Research Group, across multiple labs
  • Data sources connected and validated
  • Onboarding and training for each group
  • Named support contact

Institution

Multiple departments, a clinical and translational science institute (CTSI), or a whole health system

  • Everything in Department, across multiple departments
  • Central governance, provisioning, and usage reporting
  • Deployment reviewed with your IT security and privacy office
  • Research Camp participation and co-authorship
Frequently asked questions

Do you sign a BAA?

Yes. We execute a Business Associate Agreement as part of onboarding, alongside whatever data use agreement your privacy office requires.

How does this fit our IRB protocol?

TrialMind is analysis software; it does not change your protocol or your approvals. Analyses run under your existing IRB approval, and every cohort definition and analysis step has a reproducible audit trail.

How are seats allocated across a department?

Seats are pooled at the department or research-group level and shared across principal investigators, fellows, and graduate students. You allocate them internally; we do not meter per individual.

Can we pay from a grant or a recharge account?

Yes. We invoice against departmental research funds, Clinical and Translational Science Awards (CTSA), and training grants, and can work under a core-facility recharge model. We follow your fiscal year.

Do you support teaching and trainee onboarding?

Yes. A department license includes onboarding for each cohort of trainees and teaching material built around real study workflows rather than practice datasets.

Is co-authorship or methods collaboration available?

Yes, through our Research Camps. We co-develop and validate methods with participating institutions and publish the findings together.

License TrialMind for your institution

Licenses are available for a lab, a department, or a whole institution. Seats are pooled, not charged per person.

  1. 1. In production at two academic medical centers, described by organization type. Named references available under NDA.
  2. 2. An architectural property: TrialMind deploys into the institution's environment, and analyses execute where the data already lives.