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E-Book

10 Things Site Staff Told Us

Site staff are the operational hands and feet of your clinical study, and much of your success relies on their success.

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Case Study

Strengthening Trial Enrollment Through Pre-Screening

February 8, 2021

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E-Book

The Power of Getting Everyone in Your Clinical Trial to Work as One Team

Everyone wins when all the stakeholders of a trial work together as a team. Yet, providing this sense of camaraderie across the study ecosystem is difficult.

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Blog

How Staff Augmentation Assists with Successful Data Migration

With the goal to move active data from one system into OnCore CTMS, Advarra’s Staff Augmentation team worked with a customer’s associated hospital as it was faced with software termination.

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3 min. read
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E-Book

The Study Manager’s Guide to Cultivating Positive Site and Patient Relationships

We ask a lot of questions about what makes trials work. From speaking to clinical study sites, investigators, trial patients, and study managers, there is always a common theme: the importance of working as a team.

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Case Study

Helping to Ensure the Success of a Phase III Vaccine Trial

January 24, 2021

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E-Book

A Guide to System Integrations and Single Sign-On for Clinical Operations Teams

The growing complexity of clinical trials is being met with a new generation of eClinical tools – electronic data capture, centralized trial platforms, and risk-based management tools.

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Blog

Top 10 Educational Resources of 2020

We strive to create meaningful and relevant content for the clinical research community. Check out our top resources of 2020.

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4 min. read
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Case Study

Meeting Multiple Challenges for a Uniquely Challenging Trial

December 18, 2020

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Case Study

Demonstrating the Impact of the Longboat Portal on Recruitment Success

December 7, 2020

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Blog

Beginner’s Guide to Investigator-Initiated Trials

In investigator-initiated trials, an investigator takes on the clinical study as both the sponsor and investigator. Learn more about IITs impact on the clinical research industry.

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5 min. read
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Blog

Q&A – The Must-Haves of FDA and Common Rule Reporting Requirements

Find out more about what to report to whom--and when--in the Q&A blog follow-up to our recent webinar. Read the answers to popular audience questions:

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6 min. read
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