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Clinical Operations Team Solutions

Actionable insights keep sponsor studies on track toward successful completion.

Key Takeaway

ClinOps VPs, Study Managers, CRA Managers—and sponsors—are often frustrated by missing data and error-prone manual workflows. Saama solves these problems by automating oversight and collaboration across studies and systems at every stage.


  • Highlight enrollment issues and funnel leakage
  • Identify site-level performance issues that might introduce risk
  • Compare study performance across sponsors
  • Improve CRA productivity and performance

Operations Insights

Track the status of your clients’ studies in real time and proactively identify issues that could cause milestone delays.

  • Integrate and harmonize data from CTMS, EDC, ePRO, IxRS, and other data systems into a unified study data model
  • Quickly identify and address issues to optimize study start-up, enrollment, and compliance
  • Allows you to dynamically converse with your data through an AI-powered virtual assistant
  • Use historical data patterns to predict future outcomes
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Risk Based Monitoring

Go beyond traditional site operations with a centralized database that lowers costs and saves time.

  • Reduce compliance and regulatory risk through early notification of site issues
  • Allocate site visitation resources more effectively
  • Use custom KRIs and root-cause analysis to identify and address issues more quickly
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Saama can put you on the fast track to clinical trial process innovation.