Senior Editor, Consent Form Development

🕒 September 4

🇺🇸 United States – Remote

💵 $66.8k - $116.1k / year

⏰ Full Time

🟠 Senior

✏️ Editor

👻 Ghost score 21%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Advarra

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 1983

💼 Consulting

📦 Logistics

📣 Marketing

Consulting • Logistics • Marketing

Advarra is a provider of integrated technology and services for clinical research, combining institutional review and compliance services with software platforms to support the full clinical trial lifecycle. The company offers ethics review services (IRB, IBC, DMC, endpoint adjudication), site enablement and research staffing, and a suite of cloud products — including eRegulatory, eConsent, eSource/EDC, CTMS and study design tools — plus an AI-powered operational intelligence engine (Braid) to streamline trial start-up, enrollment, and operations. Advarra serves sponsors, CROs, research sites, and institutions with a focus on patient protection, regulatory compliance, and accelerating trial outcomes.

📋 Description

• Conduct accurate pre-review of new and revised consent forms for regulatory and operational compliance • Edit consent forms to ensure regulatory compliance and alignment with Advarra standards • Apply negotiated sponsor and site language according to client agreements and mandatory language documents • Collaborate with board members and staff to incorporate required stakeholder edits • Complete informed consent quality-control checks for self and others • Mentor new team members as requested • Maintain and increase knowledge of U.S. and/or Canadian human-subject protection, drug, device, and cosmetic research regulations and guidelines • Complete recurring Human Subjects Research Training, such as CITI • Complete organizational training as required • Attend one IRB meeting per month, or two per month during initial training • Offer process-improvement suggestions to management • Complete other duties as assigned

🎯 Requirements

• 2+ years of experience in technical/medical writing and/or editing • Bachelor’s degree • Experience writing and/or editing consent forms or other research documents • Proficiency in word processing and editing, including Tracked Changes and Compare Merge functions • Familiarity with Excel, PowerPoint, direct messaging applications such as Slack, remote meeting applications such as Zoom or RingCentral, and web-based proprietary software • 1+ years of IRB experience (preferred) • Certified IRB Professional (CIP) or completion of CIP within two years of eligibility (preferred) • Ability to communicate clearly and professionally in English, verbally and in writing • In-depth knowledge of human subjects research and informed consent • Familiarity with scientific/medical terminology and ability to convert scientific/medical information to lay terms • Ability to edit technical and/or medical documents • Ability to read and comprehend advanced technical/medical documents, including medical protocols and informed consent forms • Ability to manage multiple editing projects under conflicting demands and priorities • High attention to detail, accuracy, thoroughness, and problem-solving skills • Ability to follow written and verbal instructions and work independently • Ability to sit or stand for extended periods at a stationary workstation • Ability to regularly carry, raise, and lower objects up to 10 lbs.

🏖️ Benefits

• Variable bonus eligibility in addition to base salary • Health coverage • Paid holidays • Other benefits • Remote work arrangement