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Elevate Your Research

Advarra offers comprehensive services designed to streamline your study activation and research productivity. Maximize your investment through breakthrough efficiencies with our technology solutions and research services.

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Why Organizations Use Advarra’s Services for Sites

Accelerate Study Startup

Eliminate protocol backlogs and begin accruing patients sooner. Advarra’s extensive team and standardized processes provide fast, reliable turnaround times.

Free Up Internal Resources

Enable your staff to work on higher-value tasks. Reliable resources can be hard to retain; engage top-level professionals to fill core roles and bring necessary skills and experience to your projects

Utilize Research and Technology Experts

Maximize effectiveness by using our team’s knowledge of study activation, regulatory, and CTMS technology best practices.


Institutional Review Board (IRB) Services

IRB solutions to safeguard trial participants

Manage regulatory requirements, simplify reporting, and monitor review status in real time.

Over 3,500 institutions, hospitals, health systems, and academic medical centers (AMCs) trust Advarra to ensure compliant research conduct for everything from single investigational sites to multiple site research consortia and therapeutic networks.

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Institutional Biosafety Committee (IBC) Services

Comprehensive review and oversight of clinical trials involving investigational products containing engineered genetic material

Is your site prepared to conduct gene therapy and mRNA-engineered vaccine research? Join the world’s largest Gene Therapy Ready site network and save 5-6 weeks off your study activation timeline.

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Professional Services

Alleviate Your Administrative Burden with Advarra’s Professional Services

Increase your research productivity, maximize your Advarra investment, and experience breakthrough efficiencies with our technology-enabled professional services.

  • Coverage Analysis: Ensure your site stays compliant with Medicare billing compliance
  • Budget Negotiation: Accelerate your timeline, alleviate budget negotiation burdens, and ensure your funding goals
  • Custom eLearning: Ensure consistent and accurate training
  • Informed Consent Development: Guarantee clinical trial documentation is compliant and easily understandable
  • Protocol Calendars: Expedite study activation with custom clinical trial management system (CTMS) calendars
  • Research Staffing Solutions: Engage top-level professionals to fill core team roles
  • EDC Study Design: Accelerate IIT portfolio with high-quality calendars and forms
  • Budget Setup: Improve implementation and timelines, enabling Advarra to manage finance-related data entry
  • Study Activation Consulting: Receive the necessary expertise, and technology solutions to improve timelines

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Institutional Research Center of Excellence

Consulting services for today’s research-intensive universities, academic medical centers, and sites
  • Research Compliance: Ensure regulatory compliance within clinical research programs
  • Research Administration: Streamline and fortify the research architecture of your health system
  • Research Operations: Site-level assistance with clinical trial operations
  • HRPP/IRB Consulting Services: Significant expertise in the implementation of compliant human research protection programs

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Related Resources

 
Blog

Making the Most of Site Training: Lessons from the Pandemic

June 2, 2021

The investigator meeting and site initiation visit (SIV) are two critical milestones marking the beginning of a clinical trial for...

Ensure that your next remote site initiation visit is both productive and useful despite the virtual setting with these tips

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3 min. read
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Blog

Improving Study Activation Time for Gene Therapy Research

May 17, 2021

Gene therapies and genetically engineered vaccines are growing exponentially and will continue to become more popular. Per a report from...

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

Q&A – Regulatory Fine Points: Exploring 21 CFR Part 11 Validation

January 14, 2021

In a recent webinar, James Riddle, Shannon Roznoski, and Stuart Cotter of Advarra presented Regulatory Fine Points: Exploring 21 CFR Part...

Advarra's experts answer audience questions from our Regulatory Fine Points: Exploring 21 CFR Part 11 Validation webinar.

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5 min. read
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