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White Paper

Understanding how to Build and Leverage a DSMB Statistical Plan

Find out about the DSMB statistician’s roles, how study design can impact DSMB analysis, and what goes into a DSMB statistical plan.

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Blog

What is a Quality IRB Review?

Measuring IRB quality is often an effort to determine whether an IRB’s actions improve research participant protections.

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Webinar

Is Your Site Ready for an FDA Inspection?

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

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Blog

Beginner’s Guide to Medicare Coverage Analysis

Medicare coverage analysis evaluates how clinical research protocol items and services are billed per federal agency guidelines.

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3 min. read
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E-Book

Trend Report: 2023 Trends Impacting Clinical Research

This report defines 2023 clinical research trends and provides an outlook for the industry moving forward.

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Blog

Developing and Implementing a Successful eConsent Process

As the industry continues to shift from brick-and-mortar trials to more convenient hybrid formats, eConsent proves to be useful.

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Blog

Why Now is the Right Time to Adopt eConsent

A valuable tool for both sites and participants, now is the right time for sites to adopt an eConsent platform.

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3 min. read
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Webinar

How to Optimize Your sIRB Experience

Find out how other institutions have used sIRB requirements as an opportunity to elevate their research programs in this webinar.

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Blog

Beginner’s Guide to Budget Negotiation

Proper trial financing ensures internal costs are covered, facilitates better negotiation, and leads to higher compliance in trials.

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Blog

Beginner’s Guide to Single IRB Mandates

More governing bodies are starting to opt for single institutional review board (sIRB) review as a way to streamline research operations.

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Blog

Medicare Coverage Analysis Worksheet

Determine whether your trial meets the requirements of the National Coverage Determination (NCD) for Routine Costs in Clinical Trials.

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5 min. read
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Blog

Your Guide to sIRB Mandates

sIRB regulations and policies have been announced and implemented to help address the challenges of conducting clinical trials involving multiple research sites.

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4 min. read
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