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Clinical Operations Team Solutions

Actionable insights keep sponsor studies on track toward successful completion.
Operations Insights
Risk Based Monitoring

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
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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.

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Terms & Conditions

By inquiring about Saama’s Database Lock in a Day, you agree to be contacted by Saama and to allow Saama to use, maintain, store, and protect your personal data in accordance with our Privacy Policy.

Eligibility details are for informational purposes only. Saama, in its sole discretion, will determine your eligibility based on the information you disclose as part of the intake process. If Saama determines that you are eligible to participate, you will be notified by separate email. Eligibility depends on certain criteria, such as the size of your company, the types of clinical trials you sponsor, and the number of patients in–and stages of–your current clinical trials.

By completing the request form, you represent that you have authority to proceed on behalf of your company. Should you agree to participate, you agree to reasonably cooperate with Saama in following the guidelines and procedures required for integrating, standardizing, and analyzing your data. Participation requires the use of our Smart Data Quality application, a technology-agnostic AI engine that sits on top of your current infrastructure. The application can be used immediately, and you’re only charged for the services you use based on a predetermined estimate.

Information you share with Saama during your participation may be anonymized and/or aggregated, and made available publicly in Saama marketing materials. This information may include: types of systems and processes involved, types of departments involved, and size and regional location of your company. Such information will never be directly associated with you, nor will you or your company be identifiable without express written permission.