x

Join Advarra

Learn more about our company team, careers, and values. Join Advarra’s Talented team to take on engaging work in a dynamic environment.

See Jobs

 
Blog

Our OnCore CTMS Vision: Building a Foundation for Success

More than two decades ago, we created OnCore CTMS. What do we have in store for the future?

Read Now
5 min. read
Read more
 
White Paper

Operationalizing Research Analytics: Today, Tomorrow, Someday

Uncover how analytics, artificial intelligence, and machine learning are reshaping the foundational elements of clinical research.

Read Now
Read more
 
E-Book

Unlocking Study Activation: 2023 Study Activation Report

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

Read Now
Read more
 
Blog

What is a Data Monitoring Committee?

In a complex clinical trial, data monitoring committees oversee interim data to ensure adequate safety monitoring.

Read Now
6 min. read
Read more
 
Blog

Improving Study Activation Time for Gene Therapy Research

With the growing popularity of gene therapy research and genetically engineered vaccines, sites need to understand study activation impacts

Read Now
5 min. read
Read more
 
White Paper

4 Modernized Functions Every Sponsor Needs for Study Startup

This white paper outlines four technology capabilities sponsors need to expedite the study startup process.

Read Now
Read more
 
White Paper

Data on the go: Mobile Application Considerations for Clinical Trials and Beyond

Find out the necessary regulatory and ethical considerations when utilizing an app or connected device in human subjects research.

Read Now
Read more
 
Case Study

University of Nebraska Medical Center Streamlines Regulatory Management and Accelerates Study Startup with Advarra eReg

Learn how Advarra eReg helps UNMC support remote monitoring and how eReg helped address prevalent challenges in clinical research.

Read Now
Read more
 
Webinar

Privacy and Confidentiality in the Age of Mobile Apps and Connected Devices

Discover how to protect participant privacy in mobile-app-based clinical research. Learn about risks and what IRBs need to consider in protocol review.

Watch Now
Read more
 
Blog

Top 3 Reasons Why Your Medical Device Needs a Clinical Trial

Interpreting evolving regulations for medical devices is a common challenge for emerging biotech companies.

Read Now
4 min. read
Read more
 
Blog

Multiple Dynamic Endpoints and the Role of Endpoint Adjudication Committees in Clinical Trials

Trial designs incorporating multiple endpoints to support efficacy are receiving increased focus from the FDA, including a recently published guidance.

Read Now
6 min. read
Read more
 
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.

Read Now
Read more