Senior Editor: Consent Form Development (Remote)

Advarra; United States; On-site; USD 67,000 - 116,000; Full time

Job summary

Advarra is seeking a Sr Editor, Consent Form Development to support IRB Services in reviewing submissions and preparing informed consent forms used in human subjects research. You will mentor new editors and contribute to projects as defined by management.

Responsibilities include pre-review for regulatory compliance, editing consent forms, applying sponsor language, and collaborating with stakeholders. A strong grasp of FDA/ICH guidance and attention to detail is essential.

Qualifications

• 2+ years of technical/medical writing/editing experience with a Bachelor’s degree.
• Experience writing and/or editing consent forms or other research documents.
• Proficiency in Word processing and editing (Tracked Changes, Compare Merge).
• Familiar with Excel, PowerPoint, Slack, Zoom/RingCentral, and web-based software.

Responsibilities

• Conduct pre-review of new and revised consent forms in regulatory compliance.
• Edit consent forms to ensure regulatory alignment with standards.
• Apply sponsor/site language to consent documents per mandatory documents.
• Collaborate with Board members and staff to include edits from stakeholders.
• Mentor new editors and contribute to additional projects as needed.
• Attend IRB meetings to enhance understanding of IRB processes.

Skills

Technical writing

Editing

Word processing

Excel

PowerPoint

Slack

Zoom/RingCentral

Web-based software

Attention to detail

Communication skills

Education

Bachelor's degree

Tools

Microsoft Word

Slack

Zoom

RingCentral

PowerPoint

Excel

Job description

Advarra is seeking a Sr Editor, Consent Form Development to support IRB Services in reviewing submissions and preparing informed consent forms used in human subjects research. You will mentor new editors and contribute to projects as defined by management.

Responsibilities include pre-review for regulatory compliance, editing consent forms, applying sponsor language, and collaborating with stakeholders. A strong grasp of FDA/ICH guidance and attention to detail is essential.