In light of growing travel restrictions due to COVID-19, clinical trial sites and sponsors must consider new ways to conduct trials that require less physical contact. Since many sponsor oversight and monitoring activities are performed on-site, remote monitoring promises an encouraging solution.
In this panel discussion, leading sites share:
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Impact and risks of COVID-19 on clinical trial site monitoring
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Options for providing remote access to clinical trial data and documentation
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Guidance and perspectives on putting remote monitoring into practice
Speakers:
- Denise Snyder, Associate Dean for Clinical Research, Duke School of Medicine
- Amanda Wright, Vice President of Partnership Development, Javara
- Jessica Collins, Associate Director, Vanderbilt Coordinating Center
- Trisha Locke, CEO at Keystone Research
- Bree Burks, Vice President of Strategy, Site Solutions, Veeva Systems
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