Resources

Site Management

Project Management & Planning for Successful Clinical Trials

Follow these project management and planning basics while conducting clinical research at your site.

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Member Scenarios: Finding a Better Way to Manage Your Cancer Center Membership

We created a way to help cancer centers demonstrate collaboration for CCSG application and renewal. Product Manager, Jeremy Shapiro, explains our process for finding a solution.

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Indiana University Melvin and Bren Simon Cancer Center sees 52% time savings with Forte Participant Payments

With an increasing number of clinical trials conducted each year, IU’s Simon Cancer Center searched for a system that would decrease clinical staff’s time spent paying study participants and reduce inefficient workflows and associated costs.

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Karmanos Cancer Institute unites operational teams and creates optimized processes with Forte Insights for OnCore

Team members at the Barbara Ann Karmanos Cancer Institute recognized the importance of operational efficiency, and investigated ways they could gather and present operational data they had already collected to identify areas of success and opportunities for growth.

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Resolutions for Your Research Organization: Start Making Data-Driven Decisions

Learn how to use data to achieve your 2018 research goals and inform future operational decisions.

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6 Signs Your Site Should Stop Building Protocol Calendars Internally

Learn the telltale signs that it’s time for your research site to consider outside help for protocol calendar builds.

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Big Ideas in Clinical Research: Predictions for the Clinical Trial Industry

Hear our expert panelists discuss their predictions for clinical research in the coming year. Discover insights on centralization of research operations, the push for more electronic solutions, adapting to changes in national standards, the growing complexity of modern trials, and much more.

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Examining the Impact and Solutions to Extremely Delayed Site Payments from Sponsors

See the results of Forte’s survey of over 120 representatives from clinical trial sites and sponsors on the causes and challenges of extremely delayed clinical trial payments.

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How to Set and Meet Expectations for Your Clinical Trials: Track Staff Effort

Learn how sites can quantify protocol complexity and anticipate resources to ensure more efficient clinical trial processes.

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How to Enable your Principal Investigators for Success

Principal Investigators are responsible for the compliant and efficient execution of a clinical trial. How can a research organization empower investigators with the tools and information to maximize their success?

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