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Blog

Q&A – Site and Patient Engagement

CEO Gadi Saarony and Deb Tatton, Parexel Senior VP of Global Clinical Operations, discuss site and patient engagement. Read more:

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6 min. read
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Blog

Q&A – The Evolving Role of Technology

CEO Gadi Saarony and Deb Tatton, Parexel Senior VP of Global Clinical Operations, discuss the evolving role of technology in research. Read more:

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Blog

Accelerating the Recovery – Design and IRB Review of Safety Monitoring Plans During COVID-19

COVID-19 is rapidly changing the way research is conducted, namely how to conduct effective participant safety monitoring at a distance. Read more:

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5 min. read
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Blog

Vendor Qualification vs Requalification Audits: What’s the Difference?

Audits to support your vendor qualification and management program should be conducted using a risk-based approach. Read more:

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4 min. read
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Blog

The Opioid Crisis in America

Combating the opioid crisis requires urgent, evidence-based approaches that address clinical, research, and education issues. Read more:

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Blog

Introducing Fireside Chats: Conversations On Burning Research Topics

Advarra is excited to introduce Fireside Chats, a series of virtual conversations. Fireside Chat is an informal conversation between an Advarra representative, and a clinical research thought leader.

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2 min. read
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Blog

Q&A – The New Normal: Considerations for Restarting Research

Experts answer some of the most popular audience questions from the recent webinar The New Normal: Considerations for Restart Research. Read more:

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7 min. read
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Blog

Q&A Part 1 – Gene Therapy Research in the Age of COVID-19

Panelists from Advarra’s inaugural virtual symposium participated in a Q&A session to address questions submitted by the audience. Read part 1:

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5 min. read
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Blog

Q&A Part 2 – Gene Therapy Research in the Age of COVID-19

Expert panelists from Advarra’s gene therapy virtual symposium address some of the most popular questions submitted by the audience. Read part 2:

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4 min. read
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Blog

Patient Engagement and the IRB

With increased efforts to engage and include patient and participant communities more closely in research, when does an IRB review become required?

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Blog

For Sponsors and Sites, the Research Restart Effort Begins With Communication

The global pandemic has changed the way we think about research. Sponsors should consider how the “new normal” will impact sites and current studies.

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4 min. read
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Blog

Trial Design in the Time of COVID-19: Complex and Efficient

Complex trial designs can eliminate less-promising investigational treatments quickly to speed development, but they remain under-utilized. Read more:

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4 min. read
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