Clinical Trial Payments
Increase site satisfaction with 30-day payments
Reduce the high cost of administering site payments and give sites confidence.
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn moreDeveloping IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn moreDeveloping IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn moreDeveloping IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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SEARCH JOBSReduce the high cost of administering site payments and give sites confidence.
From a site payments perspective, this solution has been life changing for us.
Geri Masessa
Direct of Resource Management
Bayer Healthcare
Pay your sites in 30 days as promised, consistently and transparently, all while freeing your resources for higher-level work. IQVIA Technologies' Clinical Trial Payments is a tech-enabled service offering, independent of IQVIA CRO services, that takes away the burden of making payments to sites around the world. We apply our skilled financial and technology integration teams, best practices and global reach to solve a persistent industry problem that software alone cannot handle.
in payment cycle time
in administrative burden on sponsor payments staff
in site satisfaction with payments process
in questions and disputes from sites
IQVIA’s Forecasting solution offers an advanced approach to managing and predicting site payments to ensure accuracy, compliance, and efficiency across complex, global clinical trials.
Add IQVIA Forecasting to your Clinical Trial Payments solution to improve financial transparency and planning.
The investigator payment portal provided to us with IQVIA Clinical Trial Payments is one of the most user-friendly solutions we have. It gives us all the details for the payment received and really makes it easier to reconcile all our details in a timely manner.
Mohammad Millwala
CEO of DM Clinical Research, Inc.
Communication, collaboration and transparency between sites and sponsors mean trials start up and close out faster.
Manage trial master files from planning through archive with solutions designed to improve workflow efficiency, promote collaboration, and support compliance.