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Clinical Research Data Abstractor Jobs in Wichita, KS

Tekton Research Inc

Clinical Research Coordinator

Wichita, KS · On-site

$21.50 - $28.75/hr

Clinical Research Coordinator (CRC) About Tekton Research: Tekton Research is a growth-oriented ... Utilize Electronic Data Capture (EDC) systems and Clinical Trial Management Systems (CTMS) to ...

IQVIA

Clinical Research Coordinator

Wichita, KS

$35 - $42/hr

This role is ideal for candidates with hands-on clinical research experience who are passionate about patient care, data quality, and advancing healthcare innovation. The CRC will play a critical ...

Iterative Health

Research Assistant - Wichita, KS

Wichita, KS · On-site

$17.25 - $23.75/hr

This role assists Clinical Research Coordinators across every phase of study execution from participant screening and enrollment through documentation, data entry, and compliance. The ideal candidate ...

KHSC

Assistant Professor of Research

Wichita, KS · On-site

Experience mentoring clinical faculty in research or scholarly activity * Experience with IRB submissions, study design, data analysis, manuscript development, and journal submission * Experience in ...

Labcorp

Clinical Laboratory Technologist

Wichita, KS · On-site

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... Through our unparalleled science, data, technology and laboratory network, we advance diagnostics ...

Labcorp

Clinical Laboratory Technologist

Wichita, KS

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... Through our unparalleled science, data, technology and laboratory network, we advance diagnostics ...

Labcorp

Clinical Laboratory Technologist

Wichita, KS

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... Through our unparalleled science, data, technology and laboratory network, we advance diagnostics ...

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All JobsClinical Research Data Abstractor JobsClinical Research Data Abstractor Jobs in Wichita, KS

Clinical Research Data Abstractor information

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$39

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

As of Aug 31, 2026, the average hourly pay for clinical research data abstractor in Wichita, KS is $39.48, according to ZipRecruiter salary data. Most workers in this role earn between $32.45 and $46.88 per hour, depending on experience, location, and employer.

What is a clinical research data abstractor?

A Clinical Research Data Abstractor is a professional responsible for collecting and extracting important data from medical records, clinical trials, or patient charts. They ensure that the data is accurate, complete, and entered into research databases or electronic systems. This role is vital in supporting clinical research studies by ensuring high-quality data for analysis, compliance, and reporting. Clinical Research Data Abstractors often work closely with research coordinators, physicians, and other healthcare professionals.

What skills and qualifications are needed to be a clinical research data abstractor?

To thrive as a Clinical Research Data Abstractor, you need strong attention to detail, knowledge of medical terminology, and experience with data collection, often supported by a degree in health sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and possibly certifications like ACRP-CP or SoCRA-CCRP is common. Excellent organizational skills, critical thinking, and the ability to communicate clearly with research teams help set top performers apart. These skills ensure accurate, timely data abstraction that is vital for regulatory compliance and the integrity of clinical research studies.

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

Clinical Research Data Abstractors often encounter challenges such as interpreting complex medical records, ensuring data accuracy, and navigating various electronic health record (EHR) systems. To manage these challenges, it's helpful to develop strong attention to detail, maintain up-to-date knowledge of medical terminology, and collaborate closely with clinical teams for clarification when needed. Additionally, frequent communication with data managers and adhering to standardized data abstraction protocols can greatly reduce errors and improve data quality.

What is the difference between Clinical Research Data Abstractor vs Clinical Research Coordinator?

AspectClinical Research Data AbstractorClinical Research Coordinator
Primary RoleExtracts and summarizes data from clinical trial recordsManages overall study operations and participant coordination
Required SkillsAttention to detail, data management, basic medical knowledgeRegulatory compliance, patient interaction, study oversight
Work EnvironmentData entry labs, clinical trial sites, research officesClinical sites, hospitals, research institutions
CertificationsTypically none required, but certifications like CCR can helpOften requires CCRC or similar certifications

While both roles support clinical research, the Clinical Research Data Abstractor focuses on data extraction and analysis, whereas the Clinical Research Coordinator manages study logistics and participant interactions. Understanding these differences helps in choosing the right career path or job search focus.

What are popular job titles related to Clinical Research Data Abstractor jobs in Wichita, KS?

For Clinical Research Data Abstractor jobs in Wichita, KS, the most frequently searched job titles are:

What job categories do people searching Clinical Research Data Abstractor jobs in Wichita, KS look for?

The top searched job categories for Clinical Research Data Abstractor jobs in Wichita, KS are:

What cities near Wichita, KS are hiring for Clinical Research Data Abstractor jobs?

Cities near Wichita, KS with the most Clinical Research Data Abstractor job openings:

Clinical Research Data Abstractor jobs near you
Infographic showing various Clinical Research Data Abstractor job openings in Wichita, KS as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $82,122 per year, or $39.5 per hour.

Clinical Research Coordinator

Tekton Research Inc

Wichita, KS • On-site

$21.50 - $28.75/hr

Full-time

Re-posted yesterday

Job description

Clinical Research Coordinator (CRC)

About Tekton Research:

Tekton Research is a growth-oriented clinical research organization committed to conducting high-quality clinical trials that advance medical knowledge and improve patient care. We are a collaborative, values-driven team that believes in Focus, Discipline, and Accountability. At Tekton Research, we take pride in doing excellent work while fulfilling our mission of Making Life Better.

We offer competitive compensation, comprehensive benefits, and opportunities for professional growth in a supportive and fast-paced research environment.

Position Summary:

The Clinical Research Coordinator (CRC) is responsible for the day-to-day coordination and management of clinical research studies, ensuring compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. The CRC serves as the primary liaison between investigators, sponsors, study participants, and regulatory agencies while ensuring participant safety, data integrity, and successful study execution.

This role requires excellent organizational skills, strong attention to detail, and the ability to manage multiple clinical trials simultaneously in a dynamic environment.

Key Responsibilities: 

  • Coordinate and manage all aspects of assigned clinical trials from study start-up through close-out.
  • Recruit, screen, consent, and schedule study participants according to protocol requirements.
  • Collect, process, package, and ship laboratory specimens according to protocol and sponsor requirements.
  • Maintain accurate source documentation, regulatory binders, and study records in compliance with GCP, FDA regulations, and institutional policies.
  • Monitor participant safety and promptly identify, document, and report adverse events.
  • Prepare and submit regulatory documents, including Institutional Review Board (IRB) submissions, continuing reviews, and protocol amendments.
  • Collaborate with investigators, sponsors, monitors, and study staff to ensure successful study conduct.
  • Assist with monitoring visits, sponsor audits, and regulatory inspections.
  • Utilize Electronic Data Capture (EDC) systems and Clinical Trial Management Systems (CTMS) to maintain accurate study data.
  • Ensure protocol compliance while maintaining the highest standards of participant care and research integrity.

Required Qualifications:

  • High school diploma or GED required; Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, or a related field preferred.
  • Minimum of one (1) year of Clinical Research Coordinator experience.
  • Working knowledge of Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and clinical research processes.
  • Experience with pediatric and adult phlebotomy and specimen processing.
  • Strong organizational and time management skills with the ability to prioritize multiple studies.
  • Experience maintaining regulatory documentation and source records.
  • Proficiency with Electronic Data Capture (EDC) systems and Microsoft Office applications.
  • Excellent verbal and written communication skills.
  • Ability to work independently while collaborating effectively with multidisciplinary teams.

Preferred Qualifications:

  • Current ACRP-CRC or SOCRA certification.
  • Advanced degree in Nursing, Public Health, Clinical Research, or a related healthcare field.
  • Experience working on industry-sponsored or multi-center clinical trials.
  • Familiarity with clinical monitoring, participant recruitment, and retention strategies.

Why Join Tekton Research?

At Tekton Research, you'll join a team dedicated to excellence, innovation, and improving lives through clinical research. We foster a collaborative culture where professional development is encouraged, contributions are valued, and every team member plays an important role in advancing healthcare.

If you are passionate about clinical research and committed to providing exceptional patient care, we encourage you to apply and become part of the Tekton Research team.

Apply