Associate Director Clinical Quality Assurance Jobs in California
Associate Director Clinical Quality Assurance jobs in California are among the most active in the country, concentrated in the biopharma, medical device, and clinical research sectors that anchor the state's life sciences economy. Most hiring is in San Diego, San Francisco Bay Area, and Los Angeles, where companies like Genentech, Johnson and Johnson, and AbbVie maintain established operations. The most in-demand specialties are GCP compliance, audit management, and clinical trial quality oversight. See the openings below and apply to the ones that match your experience.
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Job Summary
Immediate Hire
Home Health – Medicare Patients
We are seeking a detail-oriented and experienced Clinical Quality Assurance (QA) Specialist to join our home health team. This is an in-office position focused on reviewing Medicare home health patient charts, ensuring accurate clinical documentation, and maintaining compliance with Medicare and agency standards.
Duties
* Review OASIS assessments, including Start of Care (SOC), Resumption of Care (ROC), Recertification, and Discharge assessments, for accuracy, completeness, and consistency.
* Conduct ongoing quality assurance reviews of Medicare home health patient charts.
* Ensure patient charts are complete, accurate, organized, and up to date.
* Identify missing, incomplete, inconsistent, or overdue clinical documentation.
* Review skilled nursing and therapy visit notes to ensure documentation supports the patient’s condition, skilled needs, and established plan of care.
* Verify that OASIS responses are consistent with supporting clinical documentation, including diagnoses, functional limitations, wound assessments, medications, and other relevant findings.
* Monitor clinical documentation deadlines and follow up on outstanding charting.
* Review physician orders, plans of care (485), and other required clinical documents for completeness and appropriate signatures.
* Ensure documentation supports Medicare home health requirements, including skilled necessity and homebound status when applicable.
* Communicate with field clinicians regarding documentation deficiencies, required clarifications, and corrections.
* Follow up to ensure identified QA issues are appropriately resolved by the responsible clinician.
* Assist with maintaining charts in preparation for audits, surveys, and compliance reviews.
* Maintain accurate QA tracking and report outstanding documentation issues to management.
Qualifications
* Previous experience in Medicare-certified home health preferred.
* Strong knowledge of OASIS assessments and home health clinical documentation.
* Familiarity with Medicare home health documentation and compliance requirements.
* LVN clinical background preferred, with responsibilities assigned according to licensure and scope of practice.
* Experience with home health electronic medical record (EMR) systems.
* Excellent organizational skills and attention to detail.
* Ability to identify documentation discrepancies and communicate effectively with clinical staff.
* Ability to manage multiple patient charts and meet documentation deadlines.
Position Details
* Work Location: In-office only
* Primary Focus: Clinical QA, OASIS review, and patient chart management
* Patient Population: Medicare home health patients
Pay: $35.00 - $40.00 per hour
Expected hours: 40.0 per week
Language:
- Spanish (Required)
License/Certification:
- Licensed Vocational Nurse (California) (Required)
Work Location: In person
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Find JobsAssociate Director Clinical Quality Assurance Jobs by City in California
Where California roles are concentrated, by current openings.
Associate Director Clinical Quality Assurance Job Market in California
A snapshot from current California openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
What California Employers Look For
The qualifications that appear most often in associate director clinical quality assurance jobs across California.
- Bachelor's degree in life sciences, pharmacy, or a related field is required
- Minimum of eight years of clinical quality assurance experience in regulated environments
- Deep knowledge of FDA regulations, ICH guidelines, and GCP standards
- Proven experience leading internal and external GCP audits and inspection readiness
- Strong background managing cross-functional quality teams and CRO oversight
- Proficiency with quality management systems such as Veeva Vault or similar platforms
Associate Director Clinical Quality Assurance Jobs in California: Frequently Asked Questions
How do you become a associate director clinical quality assurance in California?
The most direct path is a bachelor's degree in a life sciences field followed by progressive clinical quality assurance experience in a regulated California biotech, pharmaceutical, or medical device environment. California does not require a state-issued license for this role, but employers consistently expect demonstrated GCP audit experience, familiarity with FDA inspection processes, and a record of managing quality teams in an IND or NDA-stage development setting.
Which companies hire associate director clinical quality assurances in California?
Companies currently hiring associate director clinical quality assurances in California include ACES ABA, Arcus Biosciences, and Arrowhead Pharmaceuticals, per current listings on Migrate Mate as of October 2026. California's dense concentration of biopharma and medical device headquarters means openings appear at both global enterprise companies and well-funded mid-stage biotech firms.
Which California cities have the most associate director clinical quality assurance jobs?
San Diego, Los Angeles, and Redwood City have the most associate director clinical quality assurance openings in California. San Diego and the Bay Area lead because they host the largest clusters of biopharma and biotech headquarters and research campuses, while Los Angeles draws openings from medical device companies and contract research organizations with Southern California operations.
Are there remote associate director clinical quality assurance jobs in California?
Yes, and they are more common than in many clinical roles, since much of the work centers on document review, audit management, and regulatory oversight rather than hands-on lab activity. About 33% of associate director clinical quality assurance openings tied to California are remote or hybrid as of October 2026, with remote arrangements most typical for audit coordination, SOP development, and CRO oversight responsibilities.
How can I get hired as a associate director clinical quality assurance in California with little or no experience?
The most realistic entry point is a quality assurance associate or clinical quality specialist role at a California biotech or CRO, where you can build direct GCP audit and inspection readiness experience. Large California employers like Gilead, Genentech, and major CROs regularly hire quality coordinators and specialists as development-track positions. Earning a credential such as a Certified Quality Auditor designation strengthens your profile when moving toward director-level consideration.
Where can I find and apply to associate director clinical quality assurance jobs in California?
You can find and apply to associate director clinical quality assurance jobs in California on Migrate Mate, which lists current California openings. Search the roles that fit your background and apply directly to the ones that match your experience and target location.
See All 14 Associate Director Clinical Quality Assurance Jobs in California
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