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Video

Video: Introduction to Data Monitoring Committees

More studies now require oversight than ever. DMCs are required when a trusted independent third party is necessary to assess clinical trials

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Webinar

Clinical Research Staffing Reprioritizations and Resourcing Strategies

Gain insights on how to work through staffing reprioritizations and options to consider when planning resourcing strategies.

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Abstract

Navigating the Ethics of Remote Research Data Collection

In this article, Luke Gelinas develops a framework to identify and address key challenges for remote research data collection.

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Infographic

When do I Need a DMC?

View our infographic to learn the basics of a data monitoring committee (DMC), also referred to as data safety monitoring board (DSMB).

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Blog

The Importance of Keeping DSMBs Independent

By ensuring the DSMB is truly independent from study conduct, sponsors make trial data more trustworthy and enhance public confidence.

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3 min. read
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Video

Introduction to Advarra Consulting

Our experts work directly with your team to accelerate product development & performance, making clinical research safer, smarter, and faster.

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Blog

Beginner’s Guide to Compliant Electronic Source Data Capture

Learn about electronic source data capture in clinical trials, relevant regulations, and best practices.

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3 min. read
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Video

Introduction to Decentralized Clinical Trials

Decentralized clinical trials and the solutions and services that support them are still taking shape in the new research landscape. Learn what they are, how they impact your responsibilities and explore solutions to challenges implementing decentralized clinical trials.

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Podcast

Wendy Tate and Dylan Rosser Talk Metrics in Clinical Research

In this podcast, we delve into the importance of data collection in clinical research and share tips to leverage metrics.

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Case Study

VERO Biotech Gains FDA Approval for Complex Drug and Device Combination

Learn more about how VERO Biotech leveraged Advarra Consulting to successfully navigate the pathway to FDA approval

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Blog

Research Equity and Enrolling Non-English Speakers

This blog explains how including participants with limited English proficiency (LEP) can help improve research access and diversity.

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4 min. read
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Virtual Event

Adapting, Adopting, and Succeeding in a Decentralized Landscape

Join a discussion on the exponential evolution of clinical trials, uncover trends observed across the industry, and hear how leading research organizations have adapted to a decentralized landscape.

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