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White Paper

Ensuring Success with Clinical Development Planning

February 11, 2022

This white paper describes how to ensure a clinical plan’s feasibility, focusing on issues that matter, and mitigates anticipated program risk.

Webinar

Increase Recruitment, Retention, and Compliance with Engaging Site Training

In this webinar, learn how site training can impact your study’s success from recruitment, retention, and compliance.

Webinar

Budgeting and Billing Compliance in Study Activation

From making do with a tight budget to taking less conventional approaches, learn how you can ensure that reliable timelines are maintained.

Blog

Considerations for IRB Review: Artificial Intelligence & Machine Learning

March 11, 2022

Read this blog to learn IRB review considerations for artificial intelligence and machine learning studies.

Blog

Data Integrity – It’s All About the Data!

September 15, 2021

This blog dives into data integrity in clinical research, including how to obtain and maintain data throughout its lifecycle.

Infographic

US Medical Device Regulation 101

September 8, 2021

Speed the review process by understanding how medical devices are classified & what the IRB must review to approve device research.

Blog

Understanding Various Decentralized Terms in Research

January 26, 2022

Virtual, remote, hybrid, decentralized, mHealth, telehealth: Find out what these terms mean for clinical research.

Blog

Local Versus Central IRBs: What’s the Difference?

March 2, 2022

Local IRBs and central IRBs are not really that different, although sIRB mandates have complicated things for local IRBs.

Blog

Phase I Oncology Clinical Trials

April 26, 2021

This blog discusses what makes Phase I oncology trials complex and what IRBs need to know as they review a Phase I trial.

Blog

Beginner’s Guide to Medicare Coverage Analysis

January 26, 2023

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

Blog

Beginner’s Guide to Investigator-Initiated Trials

November 2, 2020

In investigator-initiated trials, an investigator takes on the clinical study as both the sponsor and investigator. Learn more about IITs impact on the clinical research industry.

Blog

Considerations for Transitioning from Paper to eSource

January 10, 2022

Explore the benefits of switching from paper to eSource, tips for implementation, and how to maintain compliance.