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Remote Clinical Research Instructor Jobs in Austin, TX

IQVIA

Clinical Trial Psych Rater

Austin, TX · Remote

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services ...

IQVIA

Clinical Trial Psych Rater

Austin, TX · Remote

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services ...

IQVIA

Clinical Trial Psych Rater

Austin, TX · Remote

$62K - $156K/yr

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services ...

YO AI Labs

Biostatistician Expert - Remote

Austin, TX · Remote

$60 - $70/hr

Remote Job Type: Contractor Pay: $60-$65/hour Job Overview We are looking for an experienced Biostatistician to support clinical research projects by analyzing clinical trial data, validating ...

Magnus Medical

Field Clinical Engineer

Austin, TX · On-site +1

$110K - $115K/yr

Remote ( Central U.S.) Company background Magnus Medical is a neurotechnology company ... Provide technical input to R&D and software engineering team for development of test models and ...

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All JobsClinical Research Instructor JobsRemote Clinical Research Instructor JobsRemote Clinical Research Instructor Jobs in Austin, TX

Remote Clinical Research Instructor information

See Austin, TX salary details

$10.9K

$122.8K

$188.8K

How much do remote clinical research instructor jobs pay per year?

As of Aug 27, 2026, the average yearly pay for remote clinical research instructor in Austin, TX is $122,752.00, according to ZipRecruiter salary data. Most workers in this role earn between $35,200.00 and $173,500.00 per year, depending on experience, location, and employer.

What is the difference between Remote Clinical Research Instructor vs Remote Clinical Research Coordinator?

AspectRemote Clinical Research InstructorRemote Clinical Research Coordinator
CredentialsTypically requires a clinical research certification and teaching experienceRequires clinical research certification and experience in study coordination
Work EnvironmentPrimarily online teaching, training sessions, and curriculum developmentRemote management of clinical trials, participant coordination, and data collection
Employer & IndustryEducational institutions, training companies, pharmaceutical companiesResearch sites, pharmaceutical companies, CROs
Search & Comparison IntentUnderstanding teaching roles in clinical researchUnderstanding trial management and coordination roles

The main difference is that a Remote Clinical Research Instructor focuses on educating and training others in clinical research practices, often through online courses, while a Remote Clinical Research Coordinator manages and oversees clinical trial activities remotely. Both roles require clinical research certifications but serve different functions within the industry.

What are popular job titles related to Remote Clinical Research Instructor jobs in Austin, TX?

For Remote Clinical Research Instructor jobs in Austin, TX, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Research Instructor jobs in Austin, TX look for?

The top searched job categories for Remote Clinical Research Instructor jobs in Austin, TX are:

What cities near Austin, TX are hiring for Remote Clinical Research Instructor jobs?

Cities near Austin, TX with the most Remote Clinical Research Instructor job openings:

Remote Clinical Research Instructor jobs near you
Infographic showing various Remote Clinical Research Instructor job openings in Austin, TX as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $122,752 per year, or $59 per hour.

Clinical Research Quality Assurance Specialist III

Tekton Research Inc

Austin, TX • Remote

$37.25 - $50/hr

Full-time

Re-posted 28 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 

Apply