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How to Boost Your End-User Software Training and Support

Join us as Mike Lee of Washington University School of Medicine shares his strategy for successful end-user software training and support.

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5 Reports Your Clinical Research Site Should Be Running

Join us for this webinar as Stuart Cotter of Forte Research Systems discusses operations-related reports valuable to clinical research sites.

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Examining the NCI Cancer Center Support Grant

Join us as Forte's Regina Schwind takes us through the ins and outs of the NCI Cancer Center Support Grant.

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How to Effectively and Compliantly Advertise Clinical Trials to Potential Participants

Join us for this webinar as presenters Mel Johnson, Wendy Tate and Beth Harper discuss methods for advertising clinical trials to potential study participants.

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Best Practices for Participant-Centric Payments in Clinical Trials

Join us to hear Laura Hilty of Nimblify, Inc. discuss how to streamline your participant payment workflows.

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Learn When to Accept or Decline a Study Opportunity: It’s Ok To Say No

Join us for this webinar as Doug Cavers of ClinEdge discusses how to distinguish between studies that will contribute to your site growth and studies you should decline.

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Top 10 Ways Your Site is Leaving Money Uncollected

Join us for this webinar, where Kristi Etchberger and MaryAnn Giallombardo of Clinical Research Billing will discuss the top 10 ways sites leave money uncollected, and what you can do about it.

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How to Make Your Clinical Research Site Stand Out in a Crowded Industry

Join us for this webinar as Scott Palmese of BTC Network discusses ways to market your clinical research site and stay top-of-mind for sponsors and CROs.

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Risk-based Validation Considerations When Implementing Clinical Research Systems

Join us for this webinar as Susan Nonemaker-Cox of Essex Management discusses risk-based validation considerations when implementing clinical research systems.

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Making Your Consent Forms Readable: The Why and the How

Join us for this webinar as Wendy Tate, Director of Data Analytics at Nimblify Inc. discusses HHS and FDA requirements regarding the content of an informed consent.

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