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  The Role of Harrison IRB  

The most important role of Harrison IRB is to assist sponsors and researchers conduct clinical trials that protect the rights and welfare of research participants. Our responsibility to ensure that clinical research is safe for individuals enrolling in research is one that we do not take lightly.

Harrison IRB adheres to applicable federal, state and local laws that govern research. We believe that a partnership with the sponsor that cultivates a focus on human subject protection will result in a more in-depth review of research, both ethically as well as scientifically. Each of us at Harrison IRB believe it is a privilege to be a resource for sponsors, investigators and research participants and we are dedicated to providing a service that goes above and beyond the standards set by Federal Regulations as well as Accreditation Standards.

Harrison IRB was founded by experienced clinical research professionals who felt passionately about developing processes and procedures to conduct research with the highest ethical standards. Ethical standards, which are an important, necessary component for the review and processing of research studies have been incorporated into all of our processes and procedures.

For more information about our services and capabilities, please contact us at or by calling us at (740) 845-0814.


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Advantages of Partnering with Harrison IRB
  • The VaultTM Online Secure, IRB data review
  • Use of Technology and Project Management Tools
  • Quality Document and Version Control System
  • Online Access to all IRB-Related Documents
  • Internal Audit Program
  • Accelerate study start up timelines