Editor I, Consent Form Development

Advarra

Supports Advarra in reviewing IRB submissions and preparing consent forms for human subject research. Collaborates with Board members on compliance and regulatory adherence.

Posted 6/16/2026full-timeRemote • 🇺🇸 United StatesJuniorMid-Level💰 $50,000 - $66,974 per yearWebsite

About the role

Key responsibilities & impact

Supports the IRB Services department in the review of incoming submissions and preparation of informed consent forms (ICFs)
Conduct an accurate pre-review of new and revised consent forms in regulatory compliance
Editing new and revised consent forms to ensure regulatory compliance
Collaborating with Board members and staff to include all necessary edits to the consent form
Keeping up to date with U.S. and/or Canadian Regulations and Guidelines in Human Subject Protections
Completing standard Human Subjects Research Training, such as CITI
Attending one IRB meeting per month to enhance knowledge and understanding of IRB processes

Requirements

What you’ll need

2+ years of experience in technical, medical writing and/or editing
Associates degree

Benefits

Comp & perks

health coverage
paid holidays
variable bonus

ATS Keywords

✓ Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

technical writingmedical writingeditingregulatory complianceinformed consent formsHuman Subjects Research Training

Soft Skills

collaborationattention to detailcommunication

Certifications

CITI certification