Associate Director Clinical Quality Assurance Jobs in Madison, WI
Associate Director Clinical Quality Assurance jobs in Madison are concentrated in the biotech and pharmaceutical corridors along the East Washington Avenue Innovation District and the University Research Park on the west side, with additional demand from medical device and contract research organizations. Employers hiring right now include Catalent Pharma Solutions, Accuray, and Labcorp. Scan the live roles below and apply to whichever ones fit.
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Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve health outcomes for people. With our global scale and deep expertise, you'll do meaningful work, grow your career and make a real impact. Together, we're improving health and improving lives.
Join our Labcorp Quality department as a Toxicology Quality Auditor in Madison, WI.
Responsibilities/Duties:
- Navigate to the regulations and able to read/understand specific regulations
- Conduct basic foundational audit activities such as, but not limited to protocol review, and internal facility/process and/or supplemental inspections
- Provide timely notification to management regarding identification of critical issues
- Build and maintain successful relationships on a one-to-one basis. Answers questions relating to audit findings
- Participate in liaison meetings and audit finding negotiations
- Make suggestions for improving compliance and/or efficiency of the local QA organization and business units supported
Ensure Regulatory Compliance and Quality Assurance responsibilities, as indicated in applicable controlled documents, are followed
- Other duties as assigned by management
Minimum Required:
- Minimum: Bachelor’s Degree in Life Sciences preferred (or equivalent Life Science experience)-Experience may be substituted for education
- 2 years in a GLP/GCP regulatory environment
- Ability to apply basic relevant regulatory knowledge
- Ability to follow instruction e.g. QA documents (SOPs)
- Ability to assimilate/interpret operational documents such that audit can be performed to required level
Preferred Qualifications:
- One-year experience with GLP: 21 CFR Part 58
- Ability to critically assess data and apply procedures and regulations
- Adaptability to an ever-changing work environment
- Ability to recognize gaps in procedures and regulations and consult with more senior QA individuals
- Demonstrated ability to apply critical thinking skills
The individual in this role verifies compliance to standard operating procedures (SOPs) and regulations by performing study protocol, data, report, and in-lab phase audits (where applicable) for specific study types and gain experience by participating in internal facility/process and/or supplemental inspections. The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job. It is the responsibility of all employees to comply with all applicable regulations e.g. Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) in the performance of their role.
Why People choose to work at Labcorp?
At Labcorp, it’s our people that make us great – it’s what our clients, our partners and, most importantly, what our employees say. Here, you’ll have the opportunity to work with extraordinary people with diverse viewpoints. You’ll discover your own outstanding potential as we build an even stronger organization with industry leaders from early development to the clinic and beyond. We help our clients develop medicines that improve health and improve lives of their family and friends.
All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.
Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. For more detailed information, please click here.
Labcorp is proud to be an Equal Opportunity Employer:
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.
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Top Industries Hiring
- Science & Research
- Biotechnology & Pharmaceuticals
Associate Director Clinical Quality Assurance Jobs in Madison: Frequently Asked Questions
How do I get a associate director clinical quality assurance job in Madison?
Madison's strongest hiring comes from biotech companies, pharmaceutical manufacturers, and contract research organizations clustered around the University Research Park, East Washington Avenue corridor, and the broader Dane County life sciences ecosystem. Candidates who stand out typically bring hands-on GCP audit experience, a working knowledge of FDA 21 CFR Part 11, and familiarity with clinical trial oversight at a mid-to-large sponsor or CRO. Connections through UW-Madison's research network also open doors that applications alone don't.
Which companies hire associate director clinical quality assurances in Madison?
Employers hiring associate director clinical quality assurances in Madison right now include Catalent Pharma Solutions, Accuray, and Labcorp, based on current listings on Migrate Mate as of July 2026. Madison's hiring base leans toward life sciences companies, academic medical institutions, and specialty CROs, many of which maintain quality assurance leadership roles tied to active clinical programs.
Are there remote associate director clinical quality assurance jobs in Madison?
Yes, though with limits, since associate director clinical quality assurance roles often require on-site audits, vendor visits, and direct team oversight that reduce full-remote options. About 50% of associate director clinical quality assurance openings tied to Madison are remote or hybrid as of July 2026, with the remote-eligible share concentrated in regulatory strategy, document review, and SOP development functions rather than hands-on inspection or lab-facing responsibilities.
How can I get a associate director clinical quality assurance job in Madison with little or no experience?
The most realistic entry path in Madison is moving up through clinical quality coordinator or QA specialist roles at a local CRO or pharmaceutical company, where you build audit and inspection experience under senior oversight. Madison's UW Health system, several USWC-area biotech startups, and established CROs routinely hire at the associate or specialist level and promote from within. Volunteering for cross-functional quality improvement projects and earning a RAPS or ASQ certification strengthens a candidacy significantly in this market.
Which industries hire the most associate director clinical quality assurances in Madison?
Most associate director clinical quality assurance openings in Madison sit in Science & Research and Biotechnology & Pharmaceuticals, per current listings on Migrate Mate as of July 2026. Madison's strong concentration of university-affiliated research institutions, regional pharmaceutical manufacturers, and contract research organizations drives consistent demand for clinical quality assurance leadership across these sectors.
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