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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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Webinar

Don’t Get Caught Off Guard: Inspection Readiness for Sponsors and CROs

Discover strategies for proactively assessing compliance for an FDA Inspection Readiness visit. Address deficiencies and implement corrective actions.

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Webinar

Unlocking Global Potential: Partnering Across Varying Sites in Study Startup

Join us as Advarra experts outline how sponsor organizations can work with various site types across trials and adapt their resources accordingly.

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Webinar

Advantages and Considerations for an eRegulatory Implementation

Gain an understanding of what an eReg system is and the features available to streamline clinical trial regulatory management.

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Blog

4 Unique Challenges of Oncology Trials

Oncology research is unique in many ways, including the challenges researchers face in conducting cutting-edge trials.

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5 min. read
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Blog

Improving Study Activation Time for Gene Therapy Research

With the growing popularity of gene therapy research and genetically engineered vaccines, sites need to understand study activation impacts

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5 min. read
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Blog

What Sponsors Need to Know About Medicare Coverage Analysis

Discover the role of MCA in clinical research, its impact on study activation timelines, and how outsourcing can streamline trials.

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3 min. read
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White Paper

4 Modernized Functions Every Sponsor Needs for Study Startup

This white paper outlines four technology capabilities sponsors need to expedite the study startup process.

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Blog

Collaborating with Research Sites: Best Practices for Site Selection and Study Startup

Key strategies for successful research study startup: site selection, documentation, and effective initiation.

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4 min. read
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Webinar

Reducing Site Burden Throughout Study Startup

Learn strategies to streamline workflows across sites and sponsors, and explore success stories on how to reduce site burden.

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Blog

How Single IRB Review Mandates Help Research Sponsors

The proposed single IRB mandates will impact FDA-regulated research, potentially altering existing practices at organizations.

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4 min. read
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White Paper

Unique First-in-Human Phase I IRB Considerations you Might not Know About

An institutional review board (IRB) may ask some different questions for first-in-human (FIH) Phase I trials than later phase studies.

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Webinar

Strategies for End-user Adoption

Learn about potential solutions to help you create new adoption strategies, materials, and build training to optimize end-user acceptance.

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