Editor II, Consent Form Development

🔥 13 hours ago

🇺🇸 United States – Remote

💵 $54k - $89.1k / year

⏰ Full Time

🟢 Junior

✏️ Editor

👻 Ghost score 0%

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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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-reviews of new and revised consent forms for regulatory compliance with FDA, HHS, Health Canada, TCPS2, ICH GCP, and Advarra procedures • Edit consent forms to align with regulatory standards and Advarra document requirements • Incorporate negotiated Sponsor language into consent forms according to client agreements • Collaborate with Board members and staff to incorporate stakeholder edits • Maintain and enhance knowledge of U.S. and/or Canadian regulations and guidelines concerning human subject protections, drug, device, and cosmetic research • Complete recurring Human Subjects Research Training, such as CITI • Fulfill organizational training requirements • Attend IRB meetings to develop understanding of IRB processes • Suggest process improvements to management • Perform other assigned duties

🎯 Requirements

• 1+ 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, Slack, Zoom or RingCentral, and web-based proprietary software • Ability to communicate clearly and professionally in English, both verbally and in writing • 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 • Ability to manage multiple editing projects under conflicting demands and priorities • High attention to detail, accuracy, and thoroughness • Problem-solving skills • Ability to follow written and verbal instructions and work independently • Ability to complete Human Subjects Research Training, such as CITI • Ability to attend at least one IRB meeting per month (two per month during initial training) • Ability to sit or stand for extended periods and carry, raise, and lower objects up to 10 lbs

🏖️ Benefits

• Variable bonus eligibility • Health coverage • Paid holidays • Equal opportunity and inclusive workplace