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Blog

Enhancing Research Ethics: Understanding HRPP Staffing and the sIRB Mandate

September 27, 2023

Understand the significance of HRPP staffing despite an sIRB mandate, and how HRPP staffing maintains ethical research practices.

Blog

Optimizing a Clinical Development Program to Improve ROI

August 4, 2021

As a clinical trial moves through phases, how does the return on investment benefit study design and the program overall?

Blog

What is an sIRB and Why Does my Study Need One?

August 16, 2023

Federal requirements have shifted to require most multisite clinical trials to rely on a single IRB (sIRB) for trial oversight.

Blog

IRB Review of Coronavirus and Other Emerging Infectious Disease Research: Issues to Consider

March 10, 2020

Advarra IRB experts discuss unique issues that research involving emerging infectious diseases like coronavirus can raise for IRB review. Read more:

News

Advarra Announces New Gene Therapy Ready Site Network

January 19, 2021

Advarra Announces New Gene Therapy Ready Site Network Research involving gene therapy-based treatments can start more quickly with this collective...

Page

Secure Document Exchange

Accelerate study startup via end-to-end integration and automated, seamless exchange of research documents between sites, sponsors, and CROs.

News

Advarra Launches New Podcast Series: Advarra In Conversations With

March 23, 2021

Advarra, the leader in providing institutional review board (IRB), institutional biosafety committee (IBC), research quality and compliance consulting services, and...

Blog

Deciphering the CRC Career Path: Key Skills and Responsibilities

September 17, 2015

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

Blog

How Oncology Research Is Advancing Better Research

August 26, 2020

Innovations in oncology have sparked advancements in the clinical trial industry and empowered COVID-19 research. Read more:

Blog

FDA Inspection Readiness: After the Inspection

February 24, 2021

Preparing for an FDA inspection and enabling a site-specific process to support it is important. Learn more about what to expect and implement after an FDA inspection is completed at your institution.

News

Advarra Accelerates IRB Workflows with New Upgrades to the Center for IRB Intelligence (CIRBI) Platform

October 28, 2020

This week, Advarra will release an update to the Center for IRB Intelligence (CIRBI®) Platform, continuing our focus of accelerating...

Webinar

Research Staffing Strategies During Challenging Times

With hiring freezes, furloughs, in-person restrictions, and changes in workflows and documentation, the COVID-19 pandemic has had a significant effect on clinical research staffing. What will it look like when teams get back to work in full force? What are the risks of being understaffed? When should you look for help or change your approach to staffing?