Editor I, Consent Form Development

🔥 2 minutes ago

🇺🇸 United States – Remote

💵 $50k - $67k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

✏️ Editor

Apply Now
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Logo of Advarra

Advarra

501 - 1000 employees

Founded 1983

☁️ SaaS

💊 Pharmaceuticals

SaaS • Pharmaceuticals

Advarra is a provider of integrated regulatory oversight and clinical trial technology, combining independent IRB review and compliance services with enterprise SaaS platforms (including Braid, OnCore, Clinical Conductor, eReg, and eSource). The company delivers operational intelligence, AI-powered protocol design and automation, site collaboration, study startup and enrollment tools, and strategic enablement services to sponsors, CROs, research sites, and institutions to improve efficiency, compliance, and patient safety across the clinical trial lifecycle.

📋 Description

• 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

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

🏖️ Benefits

• health coverage • paid holidays • variable bonus

Apply Now

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