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On-Demand Webinars

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Learn the basics of working with an sIRB and gain insights for successful sIRB relationships with external IRB partners.

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Discover strategies for proactively assessing compliance for an FDA Inspection Readiness visit. Address deficiencies and implement corrective actions.

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Join us as Advarra experts outline how sponsor organizations can work with various site types across trials and adapt their resources accordingly.

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Gain an understanding of what an eReg system is and the features available to streamline clinical trial regulatory management.

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Learn strategies to streamline workflows across sites and sponsors, and explore success stories on how to reduce site burden.

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This webinar will discuss the human research protection program (HRPP) opportunities and challenges through FDA and OHRP harmonization.

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Discover how to protect participant privacy in mobile-app-based clinical research. Learn about risks and what IRBs need to consider in protocol review.

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A discussion on what IRBs must consider, what might tip the scales for a study that could go either way, and what “expedited review” means.

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Learn about potential solutions to help you create new adoption strategies, materials, and build training to optimize end-user acceptance.

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Understand the FDA’s expectations for a site inspection, GCP compliance, and maintaining study integrity.

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