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Blog

The Value of Early Engagement with Your IRB

How clinical research sponsors can make the most of their relationship with IRB partners to make research operations flow smoother

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Blog

Ideas for Managing Clinical Trial Finances Post-Pandemic

Learn how effective financial workflows are critical to managing your research in 2021 and beyond thanks to industry changes this past year.

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2 min. read
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Blog

How to Design Digital Materials for Participant Engagement

Keeping a participant informed and engaged in any study is critical. This blog outlines how we can engage participants digitally.

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3 min. read
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Blog

Beginner’s Guide to IND Safety Reporting Under 21 CFR 312(c)

Learn how to ensure compliance with FDA 21 CFR 312.32, and explore Advarra solutions that support efficient and compliant safety reporting.

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3 min. read
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Blog

Study Activation: Top Four Takeaways from Research Sites

How can sponsors leverage their relationship with their sites to ensure more efficient research?

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5 min. read
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Blog

Site-Driven Metrics: Operational Data To Improve Research

Most metrics are geared toward sponsors and CROs, find out how this ultimately impacts site research operations

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5 min. read
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Video

Virtual Investigator Meetings

Advarra’s Virtual Investigator Meetings expedite site activation and increase investigator attendance, comprehension, and engagement.

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White Paper

Vendor Management and Oversight of Clinical Trials

This white paper provides practical insights and guidance on the key concepts that will help any sponsor better manage their clinical trials.

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Podcast

Study Activation Survey Results and What it Means for Sites

In this episode, we review results from Advarra's recent survey and discuss study activation success strategies for sites.

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Blog

How to Successfully Conduct Virtual Investigator Meetings

Explore best practices to conduct virtual investigator meetings to increase comprehension and expedite site activation.

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3 min. read
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White Paper

Site Technology Guide for Facilitating GCP in Decentralized Trials

Download the white paper to learn how to adhere to Good Clinical Practices (GCP) while managing the entire decentralized trial process.

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Info Sheet

Advarra eConsent

Simplify oversight and expand remote consenting capabilities with Advarra’s 21 CFR Part 11 compliant electronic consent management system.

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