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Clinical Quality Associate Jobs in California (NOW HIRING)

MACT Health Board Inc

Quality & Compliance Associate

Sonora, CA · On-site

$27.71 - $30.19/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are seeking a detail oriented Quality & Compliance Associate for a Full Time role working in a clinical setting. As a member of the health care team, the Quality & Compliance Associate provides ...

Silver Lake Psychology

Associate Clinical Director

San Diego, CA · Remote

$85K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Assurance & Clinical Oversight * Support processes for chart reviews to ensure clinical quality, documentation accuracy, and adherence to best practices, and hold providers accountable ...

Silver Lake Psychology

Associate Clinical Director

San Diego, CA · Remote

$85K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Assurance & Clinical Oversight * Support processes for chart reviews to ensure clinical quality, documentation accuracy, and adherence to best practices, and hold providers accountable ...

Silver Lake Psychology

Associate Clinical Director

San Diego, CA · On-site

$85K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Assurance & Clinical Oversight * Support processes for chart reviews to ensure clinical quality, documentation accuracy, and adherence to best practices, and hold providers accountable ...

ARC Health

Associate Clinical Director

San Diego, CA · On-site +1

$85K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Assurance & Clinical Oversight * Support processes for chart reviews to ensure clinical quality, documentation accuracy, and adherence to best practices, and hold providers accountable ...

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Showing results 21-40

All JobsClinical Quality Associate JobsClinical Quality Associate Jobs in California

Clinical Quality Associate information

See California salary details

$12

$31

$54

How much do clinical quality associate jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical quality associate in California is $31.13, according to ZipRecruiter salary data. Most workers in this role earn between $20.87 and $41.06 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 are the most commonly searched types of Clinical Quality jobs in California?

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

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

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

Clinical Quality Associate jobs near you

Clinical - QA Associate, Clinical Studies

Medvacon Life Sciences, LLC

San Diego, CA • On-site

$33/hr

Full-time

Re-posted 19 days ago

Job description

This is an on-site contract opportunity. 3 months with potential extension
Under general supervision, performs work that is varied and that may be somewhat difficult in character, but usually involves limited responsibility. Follows established protocols and work plans. May be assisted by QA Specialists and Sr. Specialists. Comply with divisional and site Environmental Health and Safety requirements.
II.  Essential Functions:
• Responsible for inspection of incoming materials for GMP production
• Assist with packaging floor activities for primary and secondary (equipment/room approval, facility compliance, auditing, label inspection, line clearance, etc.) 
• Reviews production batch records, logbooks and other associated documents
• Performs Quality verification of just-in-time labeling activities
• Performs document issuance, scanning, filing and archival activities
• Revises SOPs, Work Instructions and Forms pertaining to their area of focus, as needed
• Assists in the execution of efficiency improvement projects with guidance
• Ensures that products are manufactured, packaged, and tested according to applicable FDA guidelines, GXPs regulations and internal SOPs
• Participates in Quality programs, procedures and controls to ensure that products conform to established standards and agency guidelines
• Ensures gathering of data, investigations and deviations are timely and compliant
• Follows all Good Documentation Practices and cGMPs to ensure compliance to applicable FDA guidelines and MHRA guidelines
• Respond and interact with internal and external clients in a professional and timely manner
• All other duties as assigned
III.  Position Requirements:
Education or Equivalent: Associate’s degree or equivalent knowledge and experience.
Experience:  Six Sigma or ASQ certification preferred.
Knowledge/Skills Requirements:  
• Ability to follow and provide a variety of instructions furnished in written, oral, diagram, or schedule form
• Must be able to use existing procedures to solve routine and non-routine problems
• Must be able to utilize all elements of the quality system to identify, classify and control the status of incoming materials
• Recognizes unmet needs within department and business
• Must anticipate and identify unmet customer needs.
• Be able to proactively address work issues at the individual and team level
• Mathematical and scientific reasoning ability
• Ability to identify aberrant data and potential quality/compliance concerns escalating to management CSD-JD-QA Associate – Clinical Supplies v1.0
• Excellent written and verbal communications skills with internal and external customers, peers and managers
• Lead by example according to our values and culture
• Ability to collaborate with peers and demonstrate leadership capabilities in a matrix environment.
• Strategy is focused on personal time management and efficiency
• Well organized with ability to multitask
• Ability to work effectively under pressure to meet deadlines Physical Requirements:
• On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 40 pounds
• Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently
• May require the use of a respirator
 

Important Notice: Protecting Your Information
Medvacon Talent Acquisition only conducts initial video interviews via Microsoft Teams or Zoom. All communication will come from an email address ending in @medvacon.com. If you receive a message that seems suspicious or is not from our official domain, please report it immediately to jobs@medvacon.com.

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