This is a fully remote position, open to applicants in United States.

📋 Description

• Assists the IRB Services department in evaluating incoming submissions and preparing informed consent forms (ICFs) utilized in human subjects research.

• Perform a precise pre-review of newly submitted and revised consent forms to ensure regulatory compliance.

• Revise new and updated consent forms to guarantee adherence to regulatory standards and conformity with Advarra operational guidelines.

• Work collaboratively with Board members and staff to incorporate all essential edits to the consent form from various stakeholders.

• Provide mentorship to new team members as needed.

• Enhance and sustain personal regulatory knowledge to support organizational compliance.

⛳️ Requirements

• At least 2 years of experience in technical or medical writing and/or editing.

• Background in writing and/or editing consent forms or other research documents.

• Strong proficiency in word processing and editing, including the use of Tracked Changes and Compare Merge features.

• Familiarity with Excel, PowerPoint, direct messaging platforms such as Slack, remote meeting tools like Zoom or RingCentral, and web-based proprietary software.