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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