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

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Case Study

Large Research Healthcare System Maintains Compliance through Internal Program Assessment

Learn how Advarra ensured compliance and maintained funding sources through internal program assessments for a large healthcare system.

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Case Study

Large Clinical Research Site Network Streamlines Study Startup with Reliable, Timely ICF Writing Services

Advarra improved startup timelines by writing compliant informed consent forms (ICFs) for a large clinical research site network.

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White Paper

Establishing and Operating a DSMB: Tips for Clinical Trial Success

This white paper shares what a data safety monitoring board's (DSMB's) role is in clinical research and how it works.

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Webinar

Developing Models to Scale Your Training Program

This webinar covers strategies for adapting your training program using in-person, live virtual, and virtual/asynchronous approaches.

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Blog

What Goes into a Charter for DSMB or Endpoint Adjudication?

This blog outlines the key elements of a DMC/EAC charter document, explaining its importance in conducting safe and compliant research.

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5 min. read
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Infographic

When Do I Need an EAC?

View this infographic to learn when do you need an endpoint adjudication committee (EAC) and what types of studies an EAC reviews.

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E-Book

Clinical Trial Superheroes

Download this eBook to learn about the individuals who dedicate their talents to give patients an opportunity for healthier and longer lives.

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Webinar

The IND Journey Phase I – Navigating Success

Explore strategies for advancing investigational new drug (IND) submissions and a comprehensive guide through Phase I of the IND journey.

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White Paper

Planning Organizational Design for Clinical Development Organizations (CDOs)

The white paper outlines key elements for clinical development organizations’ organizational redesign to improve productivity.

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Info Sheet

Cosmetic Research and IRB Review

Download the info sheet to learn about IRB review of cosmetics research, including applicable regulations and the IRB’s role.

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Blog

5 Considerations for Evaluating an eIRB System

Provide guidance for research requests to the IRB, identify the appropriate regulations, and simplify the process from submission to review.

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6 min. read
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Blog

Reuniting and Reconnecting at the 2022 Onsemble Conference

The 2022 Onsemble Conference provided an opportunity for attendees to reconnect in person and collaborate to move research forward.

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5 min. read
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