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Blog

Planning Gene Therapy Research? Plan for IBC Review

The completion of the human genome project and advances in genetic engineering have paved the way for clinical trials involving human gene transfer

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Blog

Component Analysis: Analyzing Benefits and Risks of Individual Interventions to Ensure Appropriate Research Participant Protections

A major element of any IRB review is the examination of potential benefits and risks to study participants.

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Blog

IRB Review of Adaptive Design Studies

Learn why the popularity of adaptive design in clinical research is continuing to grow!

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Blog

The Six Characteristics of an NCI-Designated Cancer Center

A key component of the CCSG is to demonstrate six major characteristics of an NCI-designated cancer center. Learn more about each characteristic.

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Blog

6 Ways Sponsors Can Improve Feasibility Questionnaires

Learn how sponsors can alleviate frustrations when it comes to clinical trial feasibility questionnaires to get the best information from sites.

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5 min. read
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Blog

“Single IRB” vs “Central IRB” – What’s the Difference?

Is there a difference between the terms sIRB and cIRB?

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Blog

The Beginner’s Guide to an Electronic Data Capture (EDC) System

An Electronic Data Capture system stores patient data collected in clinical trials. Learn the basics & functionality of EDC systems.

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Blog

Deciphering the CRC Career Path: Key Skills and Responsibilities

Interested in becoming a clinical research coordinator? Understand the key skills and experiences sites look for.

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Blog

Beginner’s Guide to Clinical Trial Performance Metrics

Learn what clinical trial performance metrics are, why they are important and which key metrics for clinical trials you should be measuring.

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Blog

How Paper and Electronic Source Data Meet ALCOA Elements

ALCOA ensures source data is safe and effective, but how does it differ for data collected on paper vs. electronically?

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Blog

Best Practices in Pre-Screening Includes Use of Technology

Explore the benefits of pre-screening potential participants before they move on to the informed consent process.

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3 min. read
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