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E-Book

A Guide to System Integrations and Single Sign-On for Clinical Operations Teams

January 11, 2021

The growing complexity of clinical trials is being met with a new generation of eClinical tools – electronic data capture, centralized trial platforms, and risk-based management tools.

E-Book

Advarra Trend Report: Current State of Trial Opportunity and Selection

August 11, 2022

Insights into the site selection process and the information sites provide as part of site feasibility questionnaire completion.

E-Book

Trend Report: 2023 Trends Impacting Clinical Research

January 24, 2023

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

E-Book

Unlocking Study Activation: 2023 Study Activation Report

October 16, 2023

Access the survey report now for current perspectives on study startup activities impacted by rapidly evolving technology and tools.

News

Advarra Announces Appointment of Elisa Cascade as Chief Product Officer

February 14, 2023

Leadership appointment demonstrates Advarra’s commitment to supporting the growth of its technology offerings across the clinical research ecosystem (COLUMBIA, MD.)...

White Paper

Improving Access to Research for Diverse and Underserved Populations

May 19, 2021

Increasing diversity and inclusion in research has long been a challenge in the clinical research community. Learn strategies to increase access to clinical trials for all.

Case Study

Large NCI-designated Hospital System Trains 400 End Users, Resulting in Increased Levels of Efficiency and Consistency

June 9, 2022

Read how this hospital system completed required trainings remotely, saving the organization time as staff learned the technology.

White Paper

What Level of Review Does Your Study Need?

January 15, 2020

In this infographic, we share useful information for investigators to know which level of IRB review likely applies to their study.

Info Sheet

Effective, Ethical Research Through Informed Consent

April 15, 2021

Obtaining the effective informed consent for individuals participating in a clinical trial is paramount to ethical research.