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Director Clinical Quality Auditor Jobs (NOW HIRING)

Ohio State University

Job Title:Clinical Quality Auditor Contingent/IRP Department:Health System Shared Services ... Position Summary Under the direction of the Director of Quality and Operations Improvement ...

Cottage Health

Director, Clinical Quality

Santa Barbara, CA · On-site

$178K - $267K/yr

CH seeks a Director of Clinical Quality to provide strategic and operational leadership for the health system's clinical quality programs. This role drives performance improvement across key quality ...

University Health

Director, Clinical Quality

San Antonio, TX · On-site

$40.87 - $91.35/hr

The Director provides expertise and directs the quality and clinical outcomes program to improve quality of patient care, meet regulatory reporting requirements, and coordinate and analyze results of ...

University Health

Director, Clinical Quality

San Antonio, TX · On-site

$40.87 - $91.35/hr

The Director provides expertise and directs the quality and clinical outcomes program to improve quality of patient care, meet regulatory reporting requirements, and coordinate and analyze results of ...

Omada Health

Senior Director, Clinical Quality

$81K - $111K/yr

Omada is seeking a Senior Director, Clinical Quality to build and lead a department-level clinical quality function with end-to-end accountability for the integrity, performance, and continuous ...

NCBiotech

Director, Clinical Quality Assurance

Raleigh, NC · On-site

$190 - $234/hr

The Director, Clinical Quality Assurance is primarily responsible for establishing and leading the Clinical QA function and providing independent oversight of Good Clinical Practices (GCP) activities ...

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How much do director clinical quality auditor jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for director clinical quality auditor in the United States is $38.60, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $32.69 per hour, depending on experience, location, and employer.

What is the difference between Director Clinical Quality Auditor vs Clinical Quality Auditor?

AspectDirector Clinical Quality AuditorClinical Quality Auditor
CredentialsTypically requires a bachelor's degree in healthcare, quality assurance, or related field; certifications like CQA or CQE are commonUsually requires similar healthcare or quality certifications; may have less emphasis on advanced degrees
Work EnvironmentOversees quality programs, manages teams, and develops policies in healthcare or pharmaceutical settingsConducts audits, reviews documentation, and ensures compliance at operational levels
Employer & IndustryHealthcare organizations, pharmaceutical companies, regulatory agenciesHospitals, clinics, pharmaceutical firms, and regulatory bodies

The main difference is that the Director Clinical Quality Auditor holds a leadership role, overseeing quality assurance programs and teams, while the Clinical Quality Auditor focuses on conducting audits and ensuring compliance at the operational level. Both roles require relevant certifications and industry experience, but the director position involves strategic oversight and management responsibilities.

What cities are hiring for Director Clinical Quality Auditor jobs?

Cities with the most Director Clinical Quality Auditor job openings:

What are the most commonly searched types of Clinical Quality Auditor jobs?

The most popular types of Clinical Quality Auditor jobs are:

What states have the most Director Clinical Quality Auditor jobs?

States with the most job openings for Director Clinical Quality Auditor jobs include:

Director Clinical Quality Auditor jobs near you
Infographic showing various Director Clinical Quality Auditor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $80,278 per year, or $38.6 per hour.

Clinical Quality Auditor

South San Francisco, CA • On-site

Astrix Inc
Recruiting and Staffing Services • 1 - 5K employees
Learn more about Astrix Incexternal

$60 - $75/hr

Full-time, Contractor

Re-posted 14 days ago

Job description

Our client is a patient-driven cardiovascular biotechnology company dedicated to advancing heart disease treatment by developing therapies that address the root causes of disease rather than managing symptoms alone.
Title: GCP Auditor
Location: Hybrid (3 days onsite, South San Francisco, CA)
Pay rate: $60-75hr+ Depends on experience
Schedule: Full-time, M-F 8am-5pm
Contract-to-hire
We are seeking a GxP Auditor to join a quality team in a contract-to-hire capacity. This role is ideal for a seasoned auditor with strong GMP experience who is looking to contribute to a growing organization while supporting and helping scale a global audit program.
Role Overview
The GxP Auditor will be responsible for executing and supporting audits across internal operations, vendors, and investigator sites, ensuring compliance with global regulatory standards. This individual will also play a key role in strengthening audit program infrastructure, supporting audit reporting, and managing CAPA lifecycle activities.
Key Responsibilities
  • Plan and conduct GxP audits (primarily GMP), including vendor and clinical/investigator site audits
  • Perform audit report reviews and ensure alignment with regulatory and quality standards
  • Support the audit lifecycle, including CAPA review, approval, and closure
  • Contribute to the development and improvement of audit program infrastructure
  • Collaborate cross-functionally with Quality and Operations teams
  • Participate in scheduled audits across multiple regions (domestic and some international travel)
  • Support upcoming GCP audits and ongoing audit planning activities
  • Travel: 20-50%

Qualifications
  • MUST be a Certified Auditor (required)
  • 5-10+ years of experience in Quality, Compliance, or GxP auditing/inspections
  • Strong working knowledge of FDA, EMA, ICH, and GMDP regulations
  • Hands-on experience conducting GMP audits (vendor and/or clinical site audits preferred)
  • Experience reviewing audit reports and managing CAPAs
  • Bachelor's or advanced degree in Life Sciences, Pharmacy, Chemistry, or related field
  • Experience in biotech/pharma environments
Preferred
  • Experience with MHRA and Health Canada regulations
  • Familiarity with Veeva and/or Smartsheets
  • Strong communication, collaboration, and stakeholder management skills

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