Editor I, Consent Forms

Job Summary

Supporting the IRB Services department, the full-time Editor I, Consent Forms will conduct pre-reviews and edits of consent forms to ensure regulatory compliance and alignment with organizational standards while working remotely in the U.S.

Key responsibilities

• Conduct pre-reviews of new and revised consent forms for regulatory compliance with applicable guidelines
• Edit consent forms to ensure alignment with Advarra document standards and apply negotiated Sponsor language as needed
• Collaborate with stakeholders to incorporate necessary edits and stay updated on relevant regulations and guidelines

Required qualifications

• 2+ years of experience in technical, medical writing, and/or editing
• Associate's degree
• Completion of standard Human Subjects Research Training, such as CITI
• Ability to attend IRB meetings for enhanced understanding of IRB processes
• Familiarity with U.S. and/or Canadian Regulations in Human Subject Protections