Senior Coordinator, Quality Control

Advarra

Quality Control Coordinator conducting QC activities on IRB and staff documentation for Advarra. Ensuring accuracy, compliance, and providing feedback to Research Services staff.

Posted 7/2/2026full-timeRemote • 🇺🇸 United StatesSenior💰 $66,767 - $116,089 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Quality Control activities and compliance with Federal laws regarding Human Subjects Research Protection. Proficient in document analysis and effective communication of errors to ensure accuracy in clinical research documentation.

Highest-signal resume keywords

Quality Control ExperienceHuman Subjects Research ProtectionCertified IRB ProfessionalDocument AnalysisMS Office Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Quality ControlDocument ReviewClinical ResearchIRB ExperienceRegulatory Compliance

Soft Skills

FlexibilityAdaptabilityClear Communication

Tools & Technologies

MS WordMS ExcelMS OutlookPowerPointSlackZoom

Certifications & Qualifications

Certified IRB Professional

Industry Keywords

Federal LawsHuman Subjects ResearchResearch ServicesQuality Standards

About the role

Key responsibilities & impact

Conduct Quality Control (QC) activities on complex IRB and staff documentation to ensure accuracy compared to primary sources
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
Participate in team and department professional and personal development initiatives

Requirements

What you’ll need

Bachelor’s degree in health science or related field
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

Benefits

Comp & perks

Health coverage
Paid holidays
Professional development opportunities