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Blog

3 Must-Haves to Deploy Remote Clinical Trials

Ensure your organization has the tools to both efficiently and compliantly implement remote modalities to best reap the benefits of DCT

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Blog

Key CTMS Capabilities to Improve Financial Management

This blog outlines what you should look for in a CTMS to maximize your organization’s return on investment.

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Webinar

Social Media for Research Recruitment: Ethical and Practical Aspects

Luke Gelinas, IRB Chairperson at Advarra, addresses ethical and practical issues involved with social media recruitment.

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Info Sheet

Effective, Ethical Research Through Informed Consent

Obtaining the effective informed consent for individuals participating in a clinical trial is paramount to ethical research.

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E-Book

Realizing the Benefit of Mobile Technology in Your Clinical Trial

The use of mobile technology has been trending since smart phones hit the mainstream over 10 years ago. But the life science industry is still in the early stages of figuring out how to use mobile devices to deliver value to clinical trial patients and sponsors.

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Blog

GCP Assessment During COVID – “Did Your Clinical Trials Remain GCP Compliant During COVID-19?”

Almost a year into the COVID-19 pandemic, analyze how IRB submissions, informed consent, and remote monitoring practices have maintained GCP compliance.

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4 min. read
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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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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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Blog

Informed Consent: When, Why, and How It’s Obtained

Aside from being a regulatory and ethical requirement, informed consent is a good way to ensure participant knowledge and develop a foundation trust between researcher and participant.

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4 min. read
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Case Study

Helping to Ensure the Success of a Phase III Vaccine Trial

January 24, 2021

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