Sr Editor, Consent Form Development

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Sr Editor, Consent Form Development based in United States. This is a specialized editing role supporting the development and review of informed consent forms used in human subjects research. You will help ensure that new and revised consent documents meet applicable regulatory requirements while remaining clear, accurate, and aligned with established operational standards. The role combines technical and medical editing expertise with knowledge of clinical research, human subject protections, and informed consent requirements. You will collaborate with Institutional Review Board (IRB) members, staff, sponsors, sites, and other stakeholders to incorporate required language and resolve document requirements. As a senior member of the team, you will also contribute to quality control, mentor newer editors, and share recommendations for improving processes. The position offers an opportunity to deepen expertise across United States and Canadian research regulations while working on documents that directly support ethical and compliant clinical research. This fully remote opportunity is well suited to a detail-oriented professional who enjoys independent work, complex technical content, and making scientific information accessible to research participants.

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