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About the Webinar

Are you heading toward a major compliance risk?

Don’t make a costly mistake underestimating the importance of workforce preparedness. The consequences of educational learning gaps are significant: it impacts sites, patients and the ability to get products to market. It couldn’t be more important in the clinical trial execution process.

In this special session, WCG is pleased to provide a platform for biotechs to learn from the experience of a peer organization and avoid the most common FDA audit finding.

You will also learn from an experienced investigator site the benefits that accrue when sponsors effectively alleviate burden in addressing workforce preparedness. They know what works to boost study staff proficiencies, reduce errors and save time.

This session includes practical and actionable steps you can take to ensure site personnel are optimally prepared and to avoid significant risks to quality and compliance.

Scroll down to meet the panelists.

Our Panelists

Wendy Curran, VP Clinical Operations, Insmed, Inc.

A sponsor who has been in your shoes and was proactive in their planning process to avoid any costly mistakes.

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Patty Leuchten, Founder, WCG Avoca

A leading voice in quality who sees the impact across the industry. She will share important insights on the risks and costs to sponsors who are ill-prepared on their training plans

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Ralph Lee, ACRP-CP, Site Director, Irvine Clinical Research

A firsthand account of the risk and unnecessary burden experienced at the site level when study training is not properly planned and executed. Understand how you can remove the administrative burden so site personnel can better focus on the clinical conduct of your study.

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Ericka Atkinson, VP of Operations, WCG Trifecta

A leader in improving the efficiency and effectiveness of site training and documentation for all clinical trials with a perspective on industry best practices that you can adopt to de-risk your development and improve relations

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