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Blog

Beginner’s Guide to Independent Asset Reviews

Learn more about independent asset reviews and how they can enhance research operations.

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Podcast

James Riddle and Barbara Schneider Delve into the Different Players Involved in Reviewing Clinical Research

In this podcast episode, we discuss the different clinical research oversight committees and functions to ensure the safety of participants.

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Blog

Why it is Critical to Have and Enforce a Data Strategy?

Understand a data strategy's role in clinical research and how enforcing one will benefit your studies.

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5 min. read
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Webinar

Do You Have Appropriate Oversight? Understanding the Role of DSMBs

Take a look at the role and function of independent DMCs from charter creation through interim data analysis to prepare your next trial.

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Blog

Optimizing a Clinical Development Program to Improve ROI

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

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4 min. read
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White Paper

Steps to Implementing a Quality Management System

This white paper outlines the full implementation process of a quality management system and how to avoid conflict by focusing on quality.

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Blog

IRB Review of Social Media Recruitment and Retention Programs

Explore how existing regulations can establish best practices in using social media for clinical research participant recruitment.

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4 min. read
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White Paper

End-to-End Approach to Clinical Development

Download our white paper for practical strategies for enhancing innovation, efficiency, and talent development in clinical research.

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Blog

The Value of Early Engagement with Your IRB

How clinical research sponsors can make the most of their relationship with IRB partners to make research operations flow smoother

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3 min. read
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Podcast

Aidan Gannon and Jessica Perry Examine the Patient-centric Revolution

In this episode, Aidan Gannon of Advarra and Jessica Perry of Moderna discuss patient centricity in clinical research.

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Blog

Beginner’s Guide to IND Safety Reporting Under 21 CFR 312(c)

Learn how to ensure compliance with FDA 21 CFR 312.32, and explore Advarra solutions that support efficient and compliant safety reporting.

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3 min. read
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Blog

Study Activation: Top Four Takeaways from Research Sites

How can sponsors leverage their relationship with their sites to ensure more efficient research?

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5 min. read
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