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Remote Clinical Research Quality Assurance Jobs (NOW HIRING)

Houston Methodist

At Houston Methodist, the Sr Quality Assurance Analyst position is responsible for working with ... clinical research activities which can be ad-hoc, remote/teleconferences, or face-to-face sessions ...

InStride Health

Clinical Research Scientist

$106K - $118K/yr

Participate in the design, execution, and quality assurance for clinical outcomes research initiatives * Manage, analyze, and interpret large clinical and operational datasets using appropriate ...

InStride Health

Clinical Research Scientist

$106K - $118K/yr

Participate in the design, execution, and quality assurance for clinical outcomes research initiatives * Manage, analyze, and interpret large clinical and operational datasets using appropriate ...

WEP Clinical

Clinical Quality Assurance Manager

Be part of a mission-driven organization dedicated to advancing clinical research and transforming ... LI-remote We may use artificial intelligence (AI) tools to support parts of the hiring process ...

WEP Clinical

Clinical Quality Assurance Manager

Be part of a mission-driven organization dedicated to advancing clinical research and transforming ... LI-remote We may use artificial intelligence (AI) tools to support parts of the hiring process ...

Mckesson

Clinical QA Auditor - Remote US

Concord, NC · Remote

By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson ... clinical research environment required; Quality Assurance Auditing experience required * Work ...

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How much do remote clinical research quality assurance jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for remote clinical research quality assurance in the United States is $42.65, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $46.88 per hour, depending on experience, location, and employer.

What is a remote clinical research quality assurance professional?

A Remote Clinical Research Quality Assurance (QA) professional is responsible for ensuring that clinical research studies comply with regulatory requirements, Good Clinical Practice (GCP) guidelines, and internal quality standards, all while working from a remote location. Their tasks often include reviewing study documentation, conducting audits, monitoring processes, and providing training to research teams to uphold data integrity and patient safety. By working remotely, these professionals leverage technology to perform their duties without being physically present at research sites, making the role more flexible and accessible.

How does a remote clinical research quality assurance professional typically collaborate with on-site study teams?

Remote Clinical Research Quality Assurance professionals often work closely with on-site study teams through regular virtual meetings, email correspondence, and shared document platforms. They review documentation, monitor compliance remotely, and provide guidance on regulatory standards. While not physically present, they build strong communication channels to address issues promptly and ensure consistent quality across all study locations. Effective collaboration requires strong organizational and interpersonal skills to bridge the distance and maintain high standards throughout the research process.

What are the key skills and qualifications needed to thrive as a remote clinical research quality assurance professional, and why are they important?

To excel in Remote Clinical Research Quality Assurance, you need a strong background in clinical research protocols, regulatory guidelines (such as GCP and FDA), and a relevant science or healthcare degree. Familiarity with electronic data capture (EDC) systems, audit management software, and certifications like Certified Clinical Research Professional (CCRP) are highly valued. Attention to detail, analytical thinking, and effective remote communication are essential soft skills for this role. These skills ensure compliance, data integrity, and seamless collaboration across geographically dispersed research teams.

What is the difference between Remote Clinical Research Quality Assurance vs Remote Clinical Research Associate?

AspectRemote Clinical Research Quality AssuranceRemote Clinical Research Associate
CertificationsGCP, QA certificationsCRA certification, GCP training
Work EnvironmentAudit and compliance focus, remote or onsiteSite monitoring, data collection, remote or onsite
Employer & Industry UsagePharma, biotech, CROs, regulatory agenciesPharma, biotech, CROs, clinical trial sites

Remote Clinical Research Quality Assurance professionals focus on ensuring compliance with regulations through audits and reviews, often working remotely. In contrast, Remote Clinical Research Associates primarily monitor clinical trial sites and collect data, with a more active role in trial execution. Both roles require GCP knowledge and are integral to clinical research, but they differ in responsibilities and work focus.

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Remote Clinical Research Quality Assurance jobs near you
Infographic showing various Remote Clinical Research Quality Assurance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $88,715 per year, or $42.7 per hour.

Clinical Research Quality Assurance Specialist III

Tekton Research Inc

Austin, TX • Remote

$37.25 - $50/hr

Full-time

Re-posted 19 days ago

Job description

Tekton Research is looking for a remote Quality Assurance Specialist III to join our team.


Position: Quality Assurance Specialist III (Full-Time/Exempt)

The Quality Assurance (QA) Specialist III is a senior-level professional responsible for leading and advancing quality assurance efforts across a clinical research site network. This role involves overseeing complex audits, driving process improvement initiatives, managing compliance risks, and serving as a key resource for regulatory readiness. The QA Specialist III acts as a subject matter expert (SME) in clinical research compliance, providing strategic guidance to ensure the integrity of clinical trials and alignment with regulatory requirements.


Reports to: Quality Assurance Manager

Job Description:


  • Conduct in-depth internal audits of clinical research activities, including investigator site files, informed consent processes, source documentation, and data integrity.
  • Evaluate compliance with GCP, ICH guidelines, FDA/EMA regulations, and sponsor requirements.
  • Oversee inspection readiness activities, including mock inspections, and act as a QA representative during regulatory inspections.
  • Identify, evaluate, and manage quality risks across the site network, prioritizing areas for mitigation.
  • Develop and oversee quality improvement plans to address systemic risks.
  • Lead root cause analyses and the development of complex Corrective and Preventive Action (CAPA) plans.
  • Monitor CAPA implementation, ensure effectiveness, and report outcomes to senior leadership.
  • Design and implement site-wide quality improvement initiatives, ensuring alignment with industry best practices.
  • Develop and update Standard Operating Procedures (SOPs), work instructions, and quality manuals.
  • Provide QA team members and clinical staff with advanced quality assurance, regulatory compliance, and auditing training.
  • Mentor junior and mid-level QA professionals, supporting their development and growth within the organization.
  • Act as a subject matter expert in regulatory requirements, providing guidance to clinical operations, regulatory affairs, and other stakeholders.
  • Collaborate with internal and external stakeholders to address quality-related issues and ensure trial integrity.
  • Prepare comprehensive audit reports and executive summaries for leadership review.
  • Analyze quality metrics to identify trends, opportunities for improvement, and areas of excellence.
  • Other duties as assigned


Required Skills/Abilities:


  • In-depth knowledge of GCP, FDA/EMA regulations, ICH guidelines, and clinical trial processes.
  • Excellent written and oral communication, attention to detail, organizational and planning skills
  • Ability to perform and maintain quality work while prioritizing and managing multiple deadlines
  • Proficiency in all Microsoft Office applications (Word, Excel, Outlook, PowerPoint)
  • Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC), or similar platforms.
  • Proven ability to conduct audits and prepare detailed audit reports.
  • Demonstrated experience leading audits and managing regulatory inspections.


Education and Experience:


  • Bachelor’s degree in Life Sciences, Health Sciences, or a related field (Master’s degree preferred).
  • 5–7 years of experience in quality assurance, clinical research, or regulatory compliance, with significant experience in a QA leadership role.
  • Experience working in a multi-site clinical research organization or network.


Physical Requirements:


  • Prolonged periods of sitting at a desk and working on a computer
  • Approximately 50% travel, with the possibility of increased travel during peak periods or as project needs demand.
  • Must be able to lift to 15 pounds at times