You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Research Associate, with a strong understanding of clinical trial processes and regulatory ...
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Research Associate, with a strong understanding of clinical trial processes and regulatory ...
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Research Associate, with a strong understanding of clinical trial processes and regulatory ...
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Research Associate, with a strong understanding of clinical trial processes and regulatory ...
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Quick apply
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Quick apply
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Quick apply
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Quick apply
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Quick apply
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Quality & Performance Improvement: Contribute to QAPI initiatives aimed at advancing patient care ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...
Quality & Performance Improvement: Contribute to QAPI initiatives aimed at advancing patient care ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...
Clinical Dietitian
Wichita, KS · On-site
Quality & Performance Improvement: Contribute to QAPI initiatives aimed at advancing patient care ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...
Clinical Dietitian
Wichita, KS · On-site
Quality & Performance Improvement: Contribute to QAPI initiatives aimed at advancing patient care ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...
Clinical Dietitian
Wichita, KS · On-site
Quality & Performance Improvement: Contribute to QAPI initiatives aimed at advancing patient care ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...
Clinical Dietitian
Wichita, KS · On-site
Quality & Performance Improvement: Contribute to QAPI initiatives aimed at advancing patient care ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...
Mgr-Physician Practice
Park, KS · On-site
... in Clinical Quality, Service Quality, Community Value and Business Literacy. Responsible for ... Associate degree in health administration, business administration, management and organizational ...
Mgr-Physician Practice
Park, KS · On-site
... in Clinical Quality, Service Quality, Community Value and Business Literacy. Responsible for ... Associate degree in health administration, business administration, management and organizational ...
Chairperson - Assoc/Full Clinical Professor
Lawrence, KS · On-site
$100 - $140/hr
... quality of the program to those served. This position will provide the opportunity to remain ... associate or full clinical professor located in Lawrence, Kansas. The appointment serves at the ...
Chairperson - Assoc/Full Clinical Professor
Lawrence, KS · On-site
$100 - $140/hr
... quality of the program to those served. This position will provide the opportunity to remain ... associate or full clinical professor located in Lawrence, Kansas. The appointment serves at the ...
At Aria Care Partners, our mission is to enrich the quality of life for every resident with passion ... Associate or bachelor's degree preferred - equivalent work experience accepted Other Qualifications
At Aria Care Partners, our mission is to enrich the quality of life for every resident with passion ... Associate or bachelor's degree preferred - equivalent work experience accepted Other Qualifications
At Aria Care Partners, our mission is to enrich the quality of life for every resident with passion ... Associate or bachelor's degree preferred - equivalent work experience accepted Other Qualifications
At Aria Care Partners, our mission is to enrich the quality of life for every resident with passion ... Associate or bachelor's degree preferred - equivalent work experience accepted Other Qualifications
... quality patient care. Follows organizational policies in providing safe patient care. Performs ... Associate Degree Nursing For ADN prepared nurses hired after February 24, 2017, must complete BSN ...
... quality patient care. Follows organizational policies in providing safe patient care. Performs ... Associate Degree Nursing For ADN prepared nurses hired after February 24, 2017, must complete BSN ...
... quality patient care. Follows organizational policies in providing safe patient care. Performs ... Associate Degree Nursing For ADN prepared nurses hired after February 24, 2017, must complete BSN ...
... quality patient care. Follows organizational policies in providing safe patient care. Performs ... Associate Degree Nursing For ADN prepared nurses hired after February 24, 2017, must complete BSN ...
Clinical Nurse CA7
Kansas City, KS · On-site
... quality patient care. Follows organizational policies in providing safe patient care. Performs ... Associate Degree Nursing For ADN prepared nurses hired after February 24, 2017, must complete BSN ...
Clinical Nurse CA7
Kansas City, KS · On-site
... quality patient care. Follows organizational policies in providing safe patient care. Performs ... Associate Degree Nursing For ADN prepared nurses hired after February 24, 2017, must complete BSN ...
At Aria Care Partners, our mission is to enrich the quality of life for every resident with passion ... Associate or bachelor's degree preferred - equivalent work experience accepted Other Qualifications
At Aria Care Partners, our mission is to enrich the quality of life for every resident with passion ... Associate or bachelor's degree preferred - equivalent work experience accepted Other Qualifications
Clinical Quality Associate information
See Kansas salary details
$11.36 - $14.81
3% of jobs
$14.81 - $18.26
18% of jobs
$18.94 is the 25th percentile. Wages below this are outliers.
$18.26 - $21.71
20% of jobs
The median wage is $23.81 / hr.
$21.71 - $25.16
15% of jobs
$25.16 - $28.61
11% of jobs
$28.61 - $32.06
4% of jobs
$34.99 is the 75th percentile. Wages above this are outliers.
$32.06 - $35.51
5% of jobs
$35.51 - $38.96
8% of jobs
$38.96 - $42.41
6% of jobs
$42.41 - $45.86
6% of jobs
$45.86 - $49.31
3% of jobs
$11
$28
$49
How much do clinical quality associate jobs pay per hour?
As of Sep 6, 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?
| Aspect | Clinical Quality Associate | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Typically a bachelor's degree in life sciences or related field; certifications like CQA are a plus | Bachelor's degree in health sciences, biology, or related field; often requires research-specific certifications |
| Work Environment | Quality assurance departments, regulatory compliance teams, pharmaceutical or biotech companies | Clinical trial sites, hospitals, research institutions |
| Employer & Industry Usage | Used in pharmaceutical, biotech, and healthcare industries focusing on quality and compliance | Common 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:
Full-time
Medical, Dental, Vision, Life, Retirement
Re-posted 16 days ago
Job description
Senior CRA / CRA II - United States - Home Based
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
What You Will Do:
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:
- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
- Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
- Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Your Profile:
You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
- Willingness to travel as required (approximately 60%)
#LI-LB1 #LI-REMOTE
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.
Are you a current ICON Employee? Please click here to apply