The Workflow Gap No One Wants to Talk About

John Paul (JP) Lee, COO, AG Mednet. McKinsey alum and Kellogg MBA, JP drives operational strategy for Judi across regulated clinical trial environments.
John Paul (JP) Lee,
COO, AG Mednet. McKinsey alum and Kellogg MBA, JP drives operational strategy for Judi across regulated clinical trial environments.

The clinical trials industry has spent billions on eClinical platforms.

And yet the most common complaint I hear from site coordinators and CRAs hasn't changed in a decade, "I don't know what to do next.”

Applied Clinical Trials published two interviews recently that name a problem we've been circling for years. In The Workflow Guidance Gap Holding Back eClinical Ecosystems, Cheryl Kole, VP of Solution Strategy at Almac Clinical Technologies, examines why eClinical platforms too often prioritize data flow over the day-to-day needs of the people using them. In The Organizational Factors That Determine Whether AI Delivers Real Efficiency Gains, Krishna Cheriath, VP and Head of Clinical Research Digital Data and AI at Thermo Fisher Scientific, outlines what separates organizations that realize meaningful AI gains from those stuck in pilot purgatory.

Both observations point to the same underlying problem.

Here's the uncomfortable truth: we've been building platforms that optimize for features, not for people. We've added AI modules. Analytics dashboards. Integration APIs. And then wondered why adoption stalls at 40%. The answer isn't more technology. It's better process intelligence.

Think about the difference between giving someone a Swiss Army knife and giving them a step-by-step guide to setting up camp. Both are useful. But only one gets the tent up before dark.

The organizations seeing real returns share a common trait: they've invested as much in workflow design and user guidance as in the underlying technology. That means:

  • Mapping processes before automating them
  • Building contextual guidance into every step
  • Not bolting on a training module after go-live and calling it done

Most eClinical platforms were built for data. Judi was built for the people managing it. Not another feature-rich platform that sits unused, but an orchestration layer that embeds process intelligence directly into the workflow, surfacing who's responsible for each step and what the compliance implications are.

When a site coordinator logs in, they don't see a dashboard full of options. They see what to do next.

The Workflow Gap No One Wants to Talk About

John Paul (JP) Lee, COO, AG Mednet. McKinsey alum and Kellogg MBA, JP drives operational strategy for Judi across regulated clinical trial environments.
John Paul (JP) Lee,
COO, AG Mednet. McKinsey alum and Kellogg MBA, JP drives operational strategy for Judi across regulated clinical trial environments.

The clinical trials industry has spent billions on eClinical platforms.

And yet the most common complaint I hear from site coordinators and CRAs hasn't changed in a decade, "I don't know what to do next.”

Applied Clinical Trials published two interviews recently that name a problem we've been circling for years. In The Workflow Guidance Gap Holding Back eClinical Ecosystems, Cheryl Kole, VP of Solution Strategy at Almac Clinical Technologies, examines why eClinical platforms too often prioritize data flow over the day-to-day needs of the people using them. In The Organizational Factors That Determine Whether AI Delivers Real Efficiency Gains, Krishna Cheriath, VP and Head of Clinical Research Digital Data and AI at Thermo Fisher Scientific, outlines what separates organizations that realize meaningful AI gains from those stuck in pilot purgatory.

Both observations point to the same underlying problem.

Here's the uncomfortable truth: we've been building platforms that optimize for features, not for people. We've added AI modules. Analytics dashboards. Integration APIs. And then wondered why adoption stalls at 40%. The answer isn't more technology. It's better process intelligence.

Think about the difference between giving someone a Swiss Army knife and giving them a step-by-step guide to setting up camp. Both are useful. But only one gets the tent up before dark.

The organizations seeing real returns share a common trait: they've invested as much in workflow design and user guidance as in the underlying technology. That means:

  • Mapping processes before automating them
  • Building contextual guidance into every step
  • Not bolting on a training module after go-live and calling it done

Most eClinical platforms were built for data. Judi was built for the people managing it. Not another feature-rich platform that sits unused, but an orchestration layer that embeds process intelligence directly into the workflow, surfacing who's responsible for each step and what the compliance implications are.

When a site coordinator logs in, they don't see a dashboard full of options. They see what to do next.

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The Workflow Gap No One Wants to Talk About

Adjudication

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Imaging

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Eligibility

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Monitoring

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DSMB

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Qualification

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Key Benefits for
The Workflow Gap No One Wants to Talk About
Trials

Key Features

Workflow

Create customized workflows per event type, even within a single protocol or program

Electronic Case Report Forms

Enable eCRFs with advanced edit checks and data validation capabilities at any point in the process

De-Identification

Integrated tools enabling removal of protected health information (PHI) from document submissions

Query Management

Manage all event-related queries within the system and keep a log of all interactions

Notifications

Advanced email and web-service notifications to users based on their role

Audit Logging

Robust and compliant audit logging of all actions within Judi

Medical Imaging

Upload, de-identify, store and review medical images as part of endpoint or event submission

Role-to-Role Communications

Specific roles or groups to chat about a case or a project, detailed audit log of all interactions

Robust Reporting Infrastructure

Library of commonly-used reports to provide visibility to a given project’s status or status across a number of projects in a program. Ad hoc reports.

Dashboards and Worklists

Standard and customizable dashboards to help users visualize worklists, case status and project health

Integration

Communicate with EDC and safety systems through a well-defined web-services API

AI-Assisted Redaction

Judi’s proprietary AI-Assisted Redaction capability automatically detects potential inclusions of PHI and flags them for review, saving time and reducing regulatory risk.

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Workflow

Create customized workflows per event type, even within a single protocol or program

Electronic Case Report Forms

Enable eCRFs with advanced edit checks and data validation capabilities at any point in the process

De-Identification

Integrated tools enabling removal of protected health information (PHI) from document submissions

Query Management

Manage all event-related queries within the system and keep a log of all interactions

Notifications

Advanced email and web-service notifications to users based on their role

Audit Logging

Robust and compliant audit logging of all actions within Judi

Medical Imaging

Upload, de-identify, store and review medical images as part of endpoint or event submission

Role-to-Role Communications

Specific roles or groups to chat about a case or a project, detailed audit log of all interactions

Robust Reporting Infrastructure

Library of commonly-used reports to provide visibility to a given project’s status or status across a number of projects in a program. Ad hoc reports.

Dashboards and Worklists

Standard and customizable dashboards to help users visualize worklists, case status and project health

Integration

Communicate with EDC and safety systems through a well-defined web-services API

See Judi in Action; Request a Demo today

Contact us today to learn more about how Judi can automate, expedite, and improve your clinical trials.

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