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Clinical Quality Associate Jobs (NOW HIRING)

Abbott

Sr. Clinical Quality Associate

Maple Grove, MN · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... Clinical Quality Associate.This position could also bebased out ofourPlano, TXsite. THIS IS AN IN-HOUSE POSITION - NO REMOTE NO RELOCATION ASSISTANCE IS AVAILABLE FOR THIS POSITION. WHAT YOU'LL DO:

Abbott

Sr. Clinical Quality Associate

Maple Grove, MN

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... Clinical Quality Associate.This position could also bebased out ofourPlano, TXsite. THIS IS AN IN-HOUSE POSITION - NO REMOTE NO RELOCATION ASSISTANCE IS AVAILABLE FOR THIS POSITION. WHAT YOU'LL DO:

Abbott

Sr. Clinical Quality Associate

Maple Grove, MN · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... Clinical Quality Associate. This position could also be based out of our Plano, TX site. THIS IS AN IN-HOUSE POSITION - NO REMOTE NO RELOCATION ASSISTANCE IS AVAILABLE FOR THIS POSITION. WHAT YOU'LL ...

Bora Pharmaceuticals

Quality Associate

Maple Grove, MN · On-site

$52K - $67K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... development, clinical and commercial manufacturing, and packaging of complex oral solid dose ... The Quality Associate issues cGMP documentation to operations in support of manufacturing and ...

Biocytogen

Quality Associate

Waltham, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are seeking a detail-oriented and motivated Quality Associate to join our team. In this role ... Experience: 0-2 years of experience in a laboratory, quality, or clinical setting (Industry ...

Biocytogen

Quality Associate

Waltham, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are seeking a detail-oriented and motivated Quality Associate to join our team. In this role ... Experience: 0-2 years of experience in a laboratory, quality, or clinical setting (Industry ...

Biocytogen

Quality Associate

Waltham, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are seeking a detail-oriented and motivated Quality Associate to join our team. In this role ... Experience: 0-2 years of experience in a laboratory, quality, or clinical setting (Industry ...

Bora Pharmaceuticals

Quality Associate

Maple Grove, MN

$52K - $67K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... development, clinical and commercial manufacturing, and packaging of complex oral solid dose ... The Quality Associate issues cGMP documentation to operations in support of manufacturing and ...

WEP Clinical

Senior Clinical Quality Assurance Associate

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Clinical Quality Assurance Associate is responsible for the oversight, implementation, and continuous improvement of GCP quality systems supporting global clinical operations across all ...

Mountain Park Health Center

Be Seen First

Clinical Quality Coordinator-Clinical Quality-Gateway

Phoenix, AZ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Works in collaboration with the Director of Clinical Quality and Operations teams to determine ... Associate degree in Nursing * Current CPR certification Preferred Qualifications: * Bachelor of ...

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Clinical Quality Associate information

See salary details

$12

$31

$55

How much do clinical quality associate jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical quality associate in the United States is $31.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.59 per hour, depending on experience, location, and employer.

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 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 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 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 cities are hiring for Clinical Quality Associate jobs?

Cities with the most Clinical Quality Associate job openings:

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

The most popular types of Clinical Quality jobs are:

What states have the most Clinical Quality Associate jobs?

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

Clinical Quality Associate jobs near you

Sr Clinical Quality Associate

Arnex Solutions LLC

Plano, TX • On-site

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Associate, Maple grove, MN, Sylmar, CA, Santa Clara, CA, Plano, TX Role Summary    

The Senior Clinical Quality Associate supports clinical affairs personnel globally in ensuring compliance with medical device and Google Cloud Platform regulations and standards, as well as applicable company policies and procedures. This role spans study support, CAPA management, and internal/external audit preparation and execution.

Key Responsibilities    

•       Reviews study documents for compliance with applicable regulations, standards, and internal procedures.

•       Acts as a compliance resource to clinical study teams regarding applicable regulations, standards, and procedures.

•       Supports compliant execution of clinical research projects.

•       Generates CAPA documentation including investigations, resolution plans, and implementation reports; drives resolution cross-functionally.

•       Drives continuous process improvement and ensures work complies with regulatory and compliance standards.

•       Serves as a key player in preparation and overall support for internal and external audits, including responding to audit findings through the CAPA process.

•       May perform internal compliance assessments and/or audits.

•       Supports project teams in preparation for regulatory authority inspections or audits.

•       May support additional clinical quality tasks as needed.

Required Qualifications    

•       Bachelor’s degree in a related field, or an equivalent combination of education and work experience.

•       Minimum 4 years of related work experience with a solid understanding of clinical quality or Google Cloud Platform compliance functions.

•       Strong understanding of Good Clinical Practice (Google Cloud Platform) including U.S. regulations (21 CFR Parts 50, 54, 56, 812) and international standards (ISO 14155).

•       Strong written communication skills and independent decision-making ability.

•       Effective problem-solving and planning skills; able to work independently under minimal supervision.

Preferred Qualifications    

•       Minimum 5 years of experience in medical devices, clinical research, or a related industry.

•       Minimum 3 years in a quality role within a medical device or clinical trial environment.

•       Google Cloud Platform audit experience strongly preferred.

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