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E-Book

Improving Site-Sponsor Relationships: Proactive Strategies for Transparent Clinical Trials 

This eBook outlines how clinical research sites and sponsors can effectively work together to improve their relationship.

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Case Study

Duke University Prioritizes Advarra eReg’s Site Centric Workflows within a Connected Research Ecosystem

Download the case study to learn more about how Advarra eReg’s site centric workflows streamlined Duke University’s clinical operations.

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Blog

Navigating the FDA Emergency Use Filing Process

Partnering with Advarra, one nonprofit successfully obtained an Emergency Use Authorization from the FDA within five weeks.

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Info Sheet

Integrate Advarra’s CIRBI Platform and your electronic master file (eTMF) via Advarra Connect

Enabling Advarra Connect improves efficiency, reduces administrative burden, and streamlines audit readiness across your research portfolio.

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Blog

Developing an Emergency Preparedness Plan for your HRPP

Emergency preparedness plans help institutions plan, prepare for, and respond to emergencies as they arise.

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4 min. read
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Webinar

Didn’t Expect that to Happen: Events that must be Reported Promptly to the IRB

Upcoming: January 27

This webinar helps researchers better understand how to evaluate potentially reportable events and what needs to be reported to the IRB.

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Blog

Considerations for Transitioning from Paper to eSource

Explore the benefits of switching from paper to eSource, tips for implementation, and how to maintain compliance.

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5 min. read
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Podcast

James Riddle and Willie Muehlhausen Discuss Digital Technology and Virtual Data Collection in Clinical Research

In this episode, we discuss the growth of decentralized clinical trial technology and how IRBs evolved to account for technology advancements.

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Blog

Improving Patient Centricity and Research Access

There is an increasing challenge to find eligible patients and build trial awareness, so how should the industry address them?

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3 min. read
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Blog

For FDA Inspection Readiness, Accountability is Key

An Advarra expert provides insight in this Q&A session on the FDA inspection readiness process, including how to improve current workflows.

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3 min. read
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Blog

Unique Ethical Issues in Phase I Oncology Studies

An essential step in research, Phase I oncology studies raise unique ethical challenges for sponsors, investigators, and IRBs.

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5 min. read
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Blog

Returning to In-person Work: Sponsor Versus Site Viewpoints

An Advarra Trend Report found sites and sponsors alike are facing shifts as they continue to navigate the pandemic.

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4 min. read
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