
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.
🔥 0 minutes ago
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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.
• Conducts Quality Control (QC) activities on complex IRB and staff documentation to ensure accuracy compared to primary sources and adherence to applicable quality control standards, federal regulations, and timelines • Reviews and critically analyzes documents for accuracy in content for assigned submission types • Provides clear feedback to communicate errors to Research Services staff regarding missing and/or incomplete elements • Accomplishes daily workload priorities with flexibility and adaptability • Executes procedures in compliance with internal quality standards and external regulations • Models QC best practices through peer-to-peer training and mentorship • Participates in team and department professional and personal development initiatives
• Bachelor's degree in health science or related field, or equivalent combination of education and experience • Intermediate knowledge of Federal laws and guidelines pertaining to Human Subjects Research Protection • Two (2)+ years of IRB, clinical research or quality control experience • Proficient with MS Word, Outlook, and Excel • Familiar with PowerPoint, direct messaging applications such as Slack, remote meeting applications such as Zoom, and web-based proprietary software • Certified IRB Professional (CIP) or attainment within one (1) year of eligibility preferred
• Health coverage • Paid holidays • Other benefits
Apply Now🔥 54 minutes ago
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