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Research Assistant Position Jobs in Wichita, KS (NOW HIRING)

Iterative Health

Research Assistant - Wichita, KS

Wichita, KS · On-site

$17.25 - $23.75/hr

The Research Assistant (RA) at Iterative Health is an essential on-site member of the clinical research team, working under the direction of the Principal Investigator and site management to support ...

KHSC

Assistant Professor of Research

Wichita, KS · On-site

Why This Role Matters This position is designed to strengthen the institution's research ... Assist with internal and external grant development and help students and faculty shape scholarly ...

NAIT International

Research Associate I

Wichita, KS · On-site

$60 - $80/hr

Temporary Position This is a temporary position ending on or before August 27, 2027, with the ... The Research Associate will lead the analysis and interpretation of metagenomic datasets generated ...

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Research Assistant Position information

See Wichita, KS salary details

$7

$19

$28

How much do research assistant position jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for research assistant position in Wichita, KS is $19.60, according to ZipRecruiter salary data. Most workers in this role earn between $16.54 and $22.79 per hour, depending on experience, location, and employer.

What is the difference between Research Assistant Position vs Research Associate?

AspectResearch Assistant PositionResearch Associate
Required CredentialsBachelor's degree often required; some roles may need a master'sMaster's or Ph.D. often preferred; more specialized experience
Work EnvironmentAcademic labs, research institutions, healthcare settingsResearch labs, universities, industry R&D departments
Employer & Industry UsageUniversities, government agencies, non-profitsUniversities, private companies, biotech firms
Common Search & ComparisonOften compared for entry-level research rolesViewed as a more advanced research position

The Research Assistant Position typically involves supporting research activities under supervision, requiring a bachelor's degree. In contrast, a Research Associate usually has more experience or advanced degrees, taking on more independent responsibilities. Both roles are common in academic and research settings, but the Research Associate position generally demands a higher level of expertise and specialization.

What are popular job titles related to Research Assistant Position jobs in Wichita, KS?

For Research Assistant Position jobs in Wichita, KS, the most frequently searched job titles are:

What job categories do people searching Research Assistant Position jobs in Wichita, KS look for?

The top searched job categories for Research Assistant Position jobs in Wichita, KS are:

What cities near Wichita, KS are hiring for Research Assistant Position jobs?

Cities near Wichita, KS with the most Research Assistant Position job openings:

Research Assistant Position jobs near you
Infographic showing various Research Assistant Position job openings in Wichita, KS as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $40,768 per year, or $19.6 per hour.

Research Assistant - Wichita, KS

Iterative Health

Wichita, KS • On-site

$17.25 - $23.75/hr

Full-time

Posted 18 days ago

Key responsibilities

  • Assist the Study Team with communicating study requirements to all individuals involved in the study.

  • Assist with screening subjects for eligibility, documenting each potential participant's eligibility or exclusion, and supporting participant enrollment.

  • Help with completing study documentation, maintaining study files, entering data into eCRF and CTMS, and managing study supplies and specimen processing.

Job description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.

We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.

The Research Assistant (RA) at Iterative Health is an essential on-site member of the clinical research team, working under the direction of the Principal Investigator and site management to support the day-to-day conduct of active clinical trials. 

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 is a detail-oriented, team-first professional with a healthcare background and a genuine interest in advancing clinical research. This role is a strong entry point into the clinical research field with real exposure to the full study lifecycle. 

Where You'll Drive Impact
  • Assist the Study Team with communicating study requirements to all individuals involved in the study.
  • Work with the Study Team to develop and implement recruitment strategies in accordance with site policies and IRB requirements.
  • Assist with screening subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's eligibility or exclusion.
  • Assist with registering participants in the Clinical Trial Management System (CTMS) to ensure proper billing of study procedures to the appropriate funding source.
  • Collect and report ongoing patient recruitment and enrollment progress and metrics to site management and the PI.
  • Assist the Study Team in completing study documentation and maintaining study files in accordance with sponsor requirements and site policies, including consent forms, source documentation, case report forms, and investigational material accountability forms.
  • Enter all patient visit data in eCRF and CTMS on a daily basis or as directed.
  • Arrange secure storage of study documents in accordance with GCP guidelines or the contracted length of time, whichever is longer.
  • Maintain inventory of study supplies; follow sponsor protocol and site policies on investigational drug/device accountability when applicable.
  • Process and ship specimens per study protocol and IATA regulations as directed.
  • Work with the Study Team to manage the day-to-day activities of the study, including problem-solving, communication, and protocol management.
  • Aid the Study Team in maintaining effective and ongoing communication with sponsors, research participants, site management, and the PI throughout the course of each study.
  • Assist the Study Team in protecting the rights and welfare of all human research participants in accordance with federal regulations.
  • Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI; report instances of noncompliance to the appropriate compliance office.
  • Perform job related duties as requested 

What You Bring to the Team

  • High school diploma or equivalent required; some college coursework preferred.
  • Minimum 2 years of experience in a healthcare setting.
  • Strong written and verbal communication skills.
  • Ability to read, interpret, and apply clinic policies and research protocols.
  • Proficiency in standard office software; familiarity with CTMS or eCRF platforms a plus.
  • Highly organized with the ability to manage multiple tasks and meet deadlines.
  • Ability to work both independently and collaboratively as part of a research team.
  • Professional, detail-oriented, and committed to maintaining confidentiality and data integrity.
Preferred Qualifications
  • Prior clinical research experience or exposure to clinical trial operations.
  • Familiarity with GCP guidelines and human subject research regulations.
  • Experience with specimen processing and shipping per IATA regulations.
  • Interest in pursuing a career path in clinical research coordination or research operations.
Physical Requirements
  • Ability to sit, stand, and move throughout clinical and office environments for extended periods of time
  • Ability to lift and move up to 25 pounds as needed

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.