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Blog

Differentiating “Public” and “Private” Internet Spaces in IRB Review

The difference between “public” and “private” internet spaces has gained importance with the growing research use of internet and social media platforms as data sources. Read more:

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Blog

How Sites Can Prepare for COVID-19 Genetically Engineered Vaccine Studies

Is your site prepared to participate in COVID-19 vaccine research? Registering an IBC ahead of time gives you an advantage. Read more:

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Blog

Q&A Part 1 – Evaluating Payment to Participate in Research: Ethical and Regulatory Issues

Dr. Gelinas answers audience questions we weren’t able to address during the webinar.

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6 min. read
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Blog

Protocol Feasibility to Promote Trial Efficiency

Many studies do not accrue subjects at the site level, which contributes to a significant amount of waste of staff time and monetary resources. Read more:

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8 min. read
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Blog

Study Activation: A Complex Process That Doesn’t Have to Be Painful

If the clinical development time of a new treatment is to ever decrease, reducing the time in study activation is necessary so actual research can be done.

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3 min. read
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Blog

How Research Informs the COVID-19 Response

Research doesn’t just inform medical treatment; it informs public health and public policy, and it helps explain human behaviors. Read more:

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Blog

IRB Review of Coronavirus and Other Emerging Infectious Disease Research: Issues to Consider

Advarra IRB experts discuss unique issues that research involving emerging infectious diseases like coronavirus can raise for IRB review. Read more:

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5 min. read
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Blog

Are “Virtual Trials” Mainstream Yet?

Advarra VP of Insitutional Services James Riddle discusses using virtual trial components in traditional study designs. Read more:

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White Paper

Informed Consent: 6 Approaches to Increase Participant Comprehension

Explore six approaches for improving informed consent and supporting participants’ understanding of the studies they are asked to join.

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Blog

Key Biosafety Considerations for Coronavirus Research

Advarra Director of Biosafety Daniel Eisenman reviews opportunities, risks, and risk mitigation strategies for coronavirus research. Read more:

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7 min. read
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Blog

Revised Common Rule Compliance Now in Full Effect—and What That Means

The Revised Common Rule is here after multiple delays, exceptions, and many training sessions. As of January 20, 2020, this regulation is in full effect.

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3 min. read
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Blog

Beyond the Regulations: More Considerations for Emergency Research

Go beyond the regulatory requirements and examine three key actions research organizations must consider before conducting planned emergency research.

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7 min. read
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