Clinical Trial Manager

5 days ago


Nelson, Nelson, New Zealand SRA International Full time

Our organization is committed to maintaining the highest standards of integrity and ethics in the conduct of research. As an IRB Coordinator, you will play a critical role in ensuring that all research protocols involving human subjects are conducted in accordance with federal regulations, state laws, and University policies and procedures. The ideal candidate will have a strong understanding of human subject research protections and IRB operations, including knowledge of new or revised regulations and guidance issued by the Office for Human Subject Protections (OHRP), the Food and Drug Administration (FDA), the State of Illinois, and other regulatory agencies as applicable.

Key Performance Indicators:

  1. Ensure that all research protocols are reviewed and approved in a timely manner.
  2. Maintain accurate and detailed records of all interactions with researchers, investigators, and regulatory agencies.
  3. Develop and implement strategies to improve the efficiency and effectiveness of the IRB review process.
  4. Provide education and training to researchers, faculty, staff, and students on human subject research protections and IRB regulations.


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