Celerion24d ago

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Quality Assurance Auditor, DMB

United States·LincolnFull-Timemid

OtherQuality Assurance

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Quick Summary

Overview

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility,

Technical Tools

OtherQuality Assurance

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

Are you looking for an opportunity to be involved in creating life-saving treatments? If so, we can't wait to meet you!

Celerion, a leading global contract research organization, seeks a Quality Assurance Auditor to support our rapidly growing Data Management and Biometrics department. The successful candidate will have Quality Assurance expertise within a GCP environment. This role will be located at either our Lincoln, NE or Tempe, AZ facilities.

Role: The role of the Quality Assurance Auditor is to assess and assure study, project and process compliance with protocols, Controlled documents, and applicable regulations and guidelines through audits.

Carry out auditing of study, project, and process reports, records and data; report audit findings to operations via QA audit reports; and determine acceptability of the responses and verify the corrections (includes but not limited to Clinical Study Report audits, Protocol audits and Electronic Database Capture (EDC) audits).

Interact with internal and external clients to discuss QA observations and study-related issues; and maintain effective and professional working relationships within and across departments in relation to study projects.

Participate and lead in the improvement initiatives intended to improve quality, compliance of study, project data and reports; effectiveness and efficiency of the processes.

Detect quality issues and the need for CAPAs and evaluate deviations

Assist with the preparation for and hosting of client audits and/or regulatory inspections.

Participate in the preparation, conduct and follow-up for System Audits and Vendor Audits

Bachelor’s degree in science, IT, business, or similar

2-5 years of quality/laboratory/clinical experience

Excellent oral and written communication skills

Ability to organize and manage multiple priorities

Excellent time management skills

Attention to detail, tactful, and diplomatic

Proficiency in using electronic data and computerized systems.

Ability to travel, as needed

Celerion Values: Integrity Trust Teamwork Respect

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

Location & Eligibility

Where is the job

Lincoln, United States

Hybrid — some on-site time required

Who can apply

Listing Details

Posted: June 8, 2026
First seen: June 8, 2026
Last seen: July 3, 2026

Posting Health

Days active: 0
Repost count: 0
Trust Level: 70%
Scored at: June 8, 2026

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Celerion

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Celerion is a leading Clinical Research Organization focused on accelerating early phase drug development through innovative strategies and comprehensive research services.

Employees

3k+

Founded

2010

Domain

Jobs

External application · ~5 min on Celerion's site

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