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Clinical Quality Associate Jobs in Kansas (NOW HIRING)

Ascension

Patient Access Representative

Wichita, KS · On-site

$18.31/hr

Drive Clinical Quality: Directly contribute to the success of our Value-Based Care programs by ... associates and applicants for employment without regard to race, color, religion, sex/gender ...

Ascension

Patient Access Representative

Wichita, KS · On-site

$15.50 - $19.75/hr

Drive Clinical Quality: Directly contribute to the success of our Value-Based Care programs by ... We empower our 97,000+ associates to bring their skills and expertise every day to reimagining ...

People People

Clinical Pathology Technician

Stilwell, KS · On-site

$18.75 - $24.25/hr

Our experienced scientists provide the highest quality results coupled with segment leading ... Associate's or Bachelor's degree in Medical Laboratory Science, Biology, Animal Science, or a ...

People People

Clinical Pathology Technician

Stilwell, KS · On-site

$18.75 - $24.25/hr

Our experienced scientists provide the highest quality results coupled with segment leading ... Associate 's or Bachelor's degree in Medical Laboratory Science, Biology, Animal Science, or a ...

People People

Clinical Pathology Technician

Stilwell, KS · On-site

$18.75 - $24.25/hr

Our experienced scientists provide the highest quality results coupled with segment leading ... Associate's or Bachelor's degree in Medical Laboratory Science, Biology, Animal Science, or a ...

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Showing results 21-40

All JobsClinical Quality Associate JobsClinical Quality Associate Jobs in Kansas

Clinical Quality Associate information

See Kansas salary details

$11

$28

$49

How much do clinical quality associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical quality associate in Kansas is $28.13, according to ZipRecruiter salary data. Most workers in this role earn between $18.85 and $37.07 per hour, depending on experience, location, and employer.

What is a clinical quality associate?

Clinical Quality Associates are professionals who support the quality assurance processes within clinical trials or healthcare settings. They are responsible for ensuring that clinical practices comply with regulatory requirements, internal protocols, and industry standards. Their duties often include auditing clinical documents, monitoring study processes, and identifying areas for improvement. By maintaining high-quality standards, Clinical Quality Associates help ensure patient safety and the integrity of clinical data.

What are the key skills and qualifications needed to thrive as a clinical quality associate?

To thrive as a Clinical Quality Associate, you need a solid understanding of clinical research processes, regulatory compliance, and quality assurance principles, typically supported by a degree in life sciences or a related field. Familiarity with Good Clinical Practice (GCP) guidelines, clinical trial management systems (CTMS), and quality management software is often required. Strong attention to detail, analytical thinking, and effective communication skills make candidates stand out in this role. These skills ensure clinical trials adhere to regulatory standards and deliver reliable, high-quality data for patient safety and successful study outcomes.

What are the main challenges clinical quality associates face when ensuring compliance across multiple clinical trial sites?

Clinical Quality Associates often encounter the challenge of maintaining consistent quality and regulatory compliance across diverse clinical trial sites, each with their own procedures and personnel. Coordinating with site staff, monitoring documentation, and ensuring adherence to Good Clinical Practice (GCP) guidelines require strong communication and organizational skills. Additionally, adapting to frequent regulatory updates and handling discrepancies in real time can be demanding, but these challenges also offer opportunities to develop expertise in quality assurance processes and regulatory requirements.

What is the difference between Clinical Quality Associate vs Clinical Research Coordinator?

AspectClinical Quality AssociateClinical Research Coordinator
Required CredentialsTypically a bachelor's degree in life sciences or related field; certifications like CQA are a plusBachelor's degree in health sciences, biology, or related field; often requires research-specific certifications
Work EnvironmentQuality assurance departments, regulatory compliance teams, pharmaceutical or biotech companiesClinical trial sites, hospitals, research institutions
Employer & Industry UsageUsed in pharmaceutical, biotech, and healthcare industries focusing on quality and complianceCommon in academic, hospital, and clinical research settings

The Clinical Quality Associate primarily focuses on ensuring compliance with quality standards and regulatory requirements within the industry, while the Clinical Research Coordinator manages the day-to-day operations of clinical trials. Both roles require strong attention to detail and knowledge of clinical processes but differ in their core responsibilities and work environments.

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

The most popular types of Clinical Quality jobs in Kansas are:

What cities in Kansas are hiring for Clinical Quality Associate jobs?

Cities in Kansas with the most Clinical Quality Associate job openings:

Clinical Quality Associate jobs near you

Behavior Services & Training Support Specialist

GoodLife Innovations

Lawrence, KS • On-site

$40K - $45K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago

Job description

Behavior Services amp; Training Support Specialist
Full-Time, Salary $40,000-$45,000
GoodLife Innovations serves individuals with disabilities and aging adults across Kansas. We are seeking a Behavior Services amp; Training Support Specialist to help strengthen the quality, compliance, and day-to-day operations of our Behavior Services and Training Departments.
This is a great opportunity for someone who enjoys a mix of administrative coordination, quality assurance, and employee training. If you want your work to make a meaningful difference with a mission-driven organization, we want to hear from you!
What You'll Do:
  • Behavior Services Support
    • Review behavior service documentation for accuracy, completeness, and timeliness.
    • Support Human Rights Committee (HRC) documentation, tracking, meetings, and compliance.
    • Enter and update information in agency systems and generate reports.
    • Assist leadership with tracking clinical quality indicators and preparing meeting materials.
  • Training Support
    • Coordinate weekly new hire training and assist with training logistics.
    • Prepare training materials, classroom resources, and supplies.
    • Monitor employee training requirements and identify missing, incomplete, or expired training.
    • Support specialized training, refresher courses, and certification programs.
    • Become certified to teach CPR/First Aid and Safety Care and facilitate these courses as needed.
Some Qualifications:
  • High school diploma or equivalent required; Associate degree preferred.
  • Experience in human services, healthcare, education, training, or administrative support preferred.
  • Experience working with individuals with intellectual and developmental disabilities (IDD) preferred.
  • Comfortable learning electronic databases and documentation systems.
  • Ability to provide effective and engaging training for small and medium-sized groups.
  • Ability to maintain confidentiality and professionalism.
  • Ability to physically perform the functions of the job required.
  • Ability to work in-office and travel between regional GoodLife locations as needed.
Benefits Include:
  • Weekly pay
  • Health/dental/vision/life insurance options
  • Flexible spending account (FSA)
  • Paid time-off
  • Matching 401k
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