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Remote Clinical Data Abstractor Jobs in Austin, TX

YO AI Labs

Medical Coder - Remote

Austin, TX · Remote

$50 - $80/hr

Analyze clinical documentation and identify coding-related ambiguities or inconsistencies ... Collaborate with project teams through written and verbal communication to improve AI training data ...

YO AI Labs

Medical Coder - Remote

Austin, TX · Remote

$50 - $80/hr

Analyze clinical documentation and identify coding-related ambiguities or inconsistencies ... Collaborate with project teams through written and verbal communication to improve AI training data ...

YO AI Labs

Medical Coder - Remote

Austin, TX · Remote

$50 - $80/hr

Analyze clinical documentation and identify coding-related ambiguities or inconsistencies ... Collaborate with project teams through written and verbal communication to improve AI training data ...

Ascension

Licensed Clinical Social Worker

Austin, TX · Remote

$73K - $106K/yr

Partially Remote; may require occasional travel to facilities to meet with staff and clinicians ... Create Tailored Treatment Plans based on specialized clinical findings, translating data into ...

Tuesday Health

Clinical Supervisor (Texas)

Austin, TX · Remote

Remote (must be located in Texas), Travel required up to 30% Who We Are: Tuesday Health is a value ... Skilled in data-driven quality improvement and performance monitoring * Demonstrated leadership ...

YO AI Labs

Pharmacovigilance Expert - Remote

Austin, TX · Remote

$70 - $80/hr

Author and review evaluation tasks based on DSURs, PSURs/PBRERs, safety data, and case-level ... Experience in clinical development safety, post-marketing surveillance, QPPV/deputy QPPV roles ...

Aledade PBC

Senior Security Engineer II - DSPM

Austin, TX · On-site +1

$113K - $155K/yr

... Records, Clinical data, etc. * Prior experience with a focus on tooling, automation, and ... remote-first culture - you've come to the right place. What Does This Mean for You? At Aledade PBC ...

Aledade PBC

Senior Security Engineer II - DSPM

Austin, TX · On-site +1

$113K - $155K/yr

... Records, Clinical data, etc. * Prior experience with a focus on tooling, automation, and ... remote-first culture - you've come to the right place. What Does This Mean for You? At Aledade PBC ...

Aledade PBC

Senior Security Engineer II - DSPM

Austin, TX · Remote

$117K - $160K/yr

... Records, Clinical data, etc. * Prior experience with a focus on tooling, automation, and ... remote-first culture - you've come to the right place. What Does This Mean for You? At Aledade PBC ...

Ascension

Certified Medical Coder

Austin, TX · On-site +1

$24.87 - $33.64/hr

Remote Facility: Seton Family of Hospitals Department/Specialty: Revenue Cycle Management Schedule ... Abstract critical clinical data from medical records to accurately assign ICD-10-CM/PCS, CPT, and ...

LivaNova

Regulatory & Clinical Specialist

Austin, TX · Remote

$85K - $95K/yr

Conduct systematic literature searches, appraisal, analysis, and summarization of data for ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

Amergis Healthcare Staffing

Clinic LPN/LVN

Austin, TX · Remote

Position Summary The Remote LVN supports digital health operations by reviewing and managing clinical documentation within a telehealth environment. This role focuses on data accuracy, chart review ...

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Remote Clinical Data Abstractor information

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How much do remote clinical data abstractor jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for remote clinical data abstractor in Austin, TX is $25.10, according to ZipRecruiter salary data. Most workers in this role earn between $18.37 and $31.68 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a remote clinical data abstractor?

To excel as a Remote Clinical Data Abstractor, you need a strong background in medical terminology, anatomy, and clinical documentation, often supported by experience in healthcare or a related degree. Familiarity with electronic health record (EHR) systems, data abstraction software, and certifications such as RHIA, RHIT, or CCS are highly valued. Attention to detail, self-motivation, and strong communication skills are essential soft skills in this remote role. These competencies ensure accurate extraction and management of clinical data, supporting compliance and quality improvement initiatives.

What are some common challenges faced by remote clinical data abstractors, and how can they be managed?

Remote Clinical Data Abstractors often encounter challenges such as managing large volumes of complex medical records, interpreting varied documentation styles, and maintaining accuracy under tight deadlines. Staying organized through effective time management and utilizing standardized abstraction guidelines can help mitigate these obstacles. Regular communication with clinical teams and ongoing training are also important for resolving ambiguities and staying updated on best practices. Adapting to a remote environment requires self-discipline, but with the right tools and support, most abstractors can excel and find satisfaction in the vital work they do.

What are popular job titles related to Remote Clinical Data Abstractor jobs in Austin, TX?

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

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

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Remote Clinical Data Abstractor jobs near you
Infographic showing various Remote Clinical Data Abstractor job openings in Austin, TX as of August 2026, with employment types broken down into 90% Full Time, 5% Part Time, and 5% Contract. Highlights an 100% Remote job distribution, with an average salary of $52,212 per year, or $25.1 per hour.

Clinical Research Quality Assurance Specialist III

Tekton Research Inc

Austin, TX • Remote

$37.25 - $50/hr

Full-time

Re-posted 4 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