Secure Clinical Trial Workflow Automation for Enterprise
Generic tools risk non-compliance. Jinba Flow lets clinical ops and IT teams build auditable, SOC II compliant trial workflows and deploy them so coordinators can execute safely in Jinba App.
Clinical trial workflow automation for clinical research coordinators, IT managers in pharma, and project managers overseeing multiple trials who need SOC II compliant, auditable, governed workflow automation without coding
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Jinba's Governed Workflow Platform for Clinical Trials
Jinba's SOC II compliant platform enables pharmaceutical and clinical research organizations to build, deploy, and execute clinical trial workflows with enterprise-grade auditability, controlled access, and reusable automation. Jinba Flow's chat-to-flow builder and visual editor let operations and IT teams codify trial protocols into governed workflows that coordinators and analysts can run safely inside Jinba App.
- Describe your trial protocol in natural language and refine it in a visual flowchart editor, converting complex SOPs into deployable, reusable workflows without writing code
- Configure routing rules and conditional logic to escalate exceptions such as protocol deviations or missing patient data to the appropriate reviewer or compliance officer automatically
- Validate incoming trial data and enrich it by connecting to existing systems and databases, ensuring every workflow step operates on accurate and complete information
- Maintain a full audit log of every workflow execution with timestamps, user actions, and decision records to meet traceability and regulatory documentation requirements
How Jinba Automates Clinical Trial Workflows
Describe a clinical trial process in natural language, for example patient data intake, protocol deviation review, or regulatory submission tracking. Jinba generates a workflow draft that your team can refine in a visual flowchart editor.
Publish the workflow as a reusable API, batch process, or MCP server with enterprise controls including SSO, RBAC, and private hosting. Governed connectors keep data within your approved infrastructure.
Clinical coordinators and analysts execute approved workflows in Jinba App via chat or auto-generated forms. Guardrails prevent unauthorized changes while audit logs capture every action for compliance.
Enterprise Ready
Control, security, and support for large organizations.
Advanced access control
Role-based permissions and SSO integration.
Organization management
Spaces, roles, and approvals for your team.
Dedicated Engineer Support
Work side-by-side with our engineers to remove blockers and accelerate your workflow development.
On-premises or private cloud hosting
Run Jinba in your own environment with full data control.
Advanced access control
Role-based permissions and SSO integration.
Audit logging
Complete compliance and security oversight tracking.
Organization management
Spaces, roles, and approvals for your team.
Pre-built & custom integrations
100+ pre-built integrations plus custom connectors for your internal systems.
Dedicated Engineer Support
Work side-by-side with our engineers to remove blockers and accelerate your workflow development.
Private model hosting
Use Bedrock, Azure AI, or your own models securely.
Build Governed Clinical Trial Workflows Your Teams Can Trust
If your trial coordination processes rely on manual handoffs and generic tools, Jinba can turn them into secure, auditable workflows that clinical ops teams can execute with confidence.
Frequently Asked Questions
Everything you need to know about Jinba. Can't find the answer you're looking for? Reach out to our support team.
Is Jinba compliant with enterprise security standards for clinical trials?
Can non-technical coordinators run clinical workflows without coding?
How does Jinba handle protocol deviations or exceptions in a trial?
Does Jinba maintain audit logs for regulatory documentation?
Can Jinba integrate with the systems our clinical teams already use?
How do we build a new clinical trial workflow in Jinba?
Can multiple teams share and reuse clinical workflows across trials?
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