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Clinical Research Administrator

2 weeks ago


Nelson, Nelson, New Zealand SRA International Full time

About the Role

The Department of Surgery at the University of Illinois Chicago is seeking an experienced Clinical Research Administrator to join their team as an IRB Coordinator. The successful candidate will provide regulatory expertise and guidance to the research community, ensuring compliance with federal and state regulations.

Key Responsibilities

  • Educate researchers on human subject research protections and IRB operations
  • Provide administrative support to the IRB, including preparing research protocol submissions and conducting regulatory reviews
  • Collaborate with researchers, clinicians, and other institutional officials to assess clinical research trials and suggest improvements

Requirements

  • Bachelor's degree in a related field and 1-2 years of experience in human subject research or 2-4 years of experience in a related area
  • Demonstrated analytical skills and knowledge of federal regulations governing human subjects research
  • Strong interpersonal and communication skills

We Offer

A dynamic and supportive work environment, opportunities for professional growth and development, and a comprehensive benefits package.