Solutions > StudyOrganizer for Sponsors

StudyOrganizer

Give Sites Everything They Need for Your Study at Their Fingertips

Deploy all of your study information including software logins, key contact information, critical study information and other important information directly to sites in one place. Track site staff changes, software logins, and key activity throughout the study.

Florence eTMF Electronic Trial Master File

How Florence’s StudyOrganizer Transforms Your Operations

Enabling sites to do their best work unlocks value for sponsors and CROs across the full research cycle.

Faster Tech Adoption

Enhance technology adoption at your sites by pre-loading all necessary study tool bookmarks and access details, placing your complete tech stack right at the fingertips of the site team.

Streamline Site Staff Onboarding

Efficiently onboard new site staff by providing immediate access to the latest trial technology and all essential study information consolidated in one convenient location.

Instant Alerts for Staff Changes

Stay ahead with real-time notifications for any additions or removals of site staff in your study, ensuring your team is always informed and every member is thoroughly trained and current.

Identify Blockers Early

Implement in-app pulse surveys to gain valuable insights into operational performance, swiftly identify and resolve issues, and monitor site engagement and satisfaction for impactful enhancements.

Deeper Insights, Empowered Oversight

Enhance CRO reporting by integrating direct, in-depth insights on study startup, satisfaction, and ongoing operations, validating the information and recommendations from your CRO, and providing clear operational oversight on your schedule.

Streamline Future Study Readiness

Enable sites to effortlessly extend the use of the solution across multiple studies, ensuring they are consistently prepared and well-trained, thereby accelerating future study operations.

In clinical research, compliance is crucial. We’ve got you covered globally.

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Why being rated #1 out of 190 clinical trial platforms on G2 by research sites matters for you.

  • High Adoption: We lead the industry with 92%+ site technology activation per study.

  • Faster Timelines: Intuitive workflows that eliminate duplicate work mean work gets done fast.

  • Low FTE Burden: You don’t need large dedicated IT teams to support implementation and management.

  • Always Reliable: Our customers have had 100% uptime over the last 12 months. We’re there when you need us.

Let’s Cure Clinical
Trials Together