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Editor I

9/23/2025

N/A

Job Summary

A company is looking for an Editor I to support the IRB Services department in reviewing submissions and preparing informed consent forms for human subject research.

Key Responsibilities
  • Conduct pre-reviews of consent forms for regulatory compliance and adherence to document standards
  • Edit consent forms and apply sponsor language as required by client agreements
  • Collaborate with stakeholders and stay updated on regulations and guidelines related to human subject protections
Required Qualifications
  • Minimum of 2 years of experience in technical or medical writing and/or editing
  • Associate degree is preferred
  • Completion of standard Human Subjects Research Training, such as CITI
  • Ability to attend IRB meetings and complete organizational training as required
  • Familiarity with U.S. and/or Canadian regulations in human subject research

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