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9 Ways to Reduce Clinical Trial Site Burden

As leaders in clinical research, sponsors can have the ability to drastically reduce elements of clinical trial site burden.
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How to Write Site-Friendly Protocol Amendments in Clinical Trials

Clinical trial protocol development and maintenance are some of the most critical steps in the lifecycle of a research study. One of the most common (and important) maintenance ...
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3 Ways Sponsors and Sites Can Improve Patient Slot Allocation in Early Phase Clinical Trials

Patient slot allocation can be a critical element of early phase clinical trials. There may be a limited number of spots in the trial for participants, and the process of enrolling ...
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4 Reasons Sites Need to Automate Processes Around Clinical Trial Billing

When you look at clinical trial site financials at a high level, gaps in invoice creation, gaps in billing, and gaps in payment reconciliation can all add up. That combination of ...
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4 Ways to Improve Patient Centricity in Clinical Trials

Not only can a patient-centric approach to clinical trials build stronger relationships between patients and their site teams for smoother workflows, it can also increase patient ...
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3 Benefits of Clinical Trial Enrollment Forecasting

By Josh Brandoff, Head of Data at OneStudyTeam
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