1

Research Assistant Lab Manager Jobs in Wichita, KS

... Assistant Professor of Research to help expand a strong culture of scholarship across the ... The ideal candidate will be someone who can manage multiple concurrent projects, provide strong ...

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... LabCorp is seeking a Lab Assistant to join our team Ascension Via Christi St. Francis Hospital in ...

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... LabCorp is seeking a Lab Assistant to join our team Ascension Via Christi St. Francis Hospital in ...

Phlebotomist/Medical Lab Assistant

Wichita, KS · On-site

$15.25 - $19/hr

In collaboration with the Lab and Radiology Manager, the Medical Lab Assistant ensures they are in compliance with all federal grants, OSHA, CLIA, and Hunter Health Clinic policies and procedures.

Phlebotomist/Medical Lab Assistant

Wichita, KS · On-site

$15.25 - $19/hr

In collaboration with the Lab and Radiology Manager, the Medical Lab Assistant ensures they are in compliance with all federal grants, OSHA, CLIA, and Hunter Health Clinic policies and procedures.

Phlebotomist/Medical Lab Assistant

Wichita, KS · On-site

$15.25 - $19/hr

In collaboration with the Lab and Radiology Manager, the Medical Lab Assistant ensures they are in compliance with all federal grants, OSHA, CLIA, and Hunter Health Clinic policies and procedures.

next page

Showing results 1-20

Research Assistant Lab Manager information

See Wichita, KS salary details

$9

$18

$26

How much do research assistant lab manager jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for research assistant lab manager in Wichita, KS is $18.11, according to ZipRecruiter salary data. Most workers in this role earn between $14.86 and $20.62 per hour, depending on experience, location, and employer.

What is a research assistant lab manager?

Research Assistant Lab Managers are professionals who oversee the daily operations of research laboratories while also assisting with scientific experiments and projects. Their responsibilities typically include managing lab supplies, maintaining equipment, ensuring safety protocols are followed, and coordinating the work of other lab staff or students. They often assist principal investigators with experiment design, data collection, and analysis. Effective lab managers balance administrative duties with hands-on research support, making them essential for efficient and safe lab environments.

What are the key skills and qualifications needed to thrive as a research assistant lab manager, and why are they important?

To thrive as a Research Assistant Lab Manager, you need a solid background in laboratory techniques, experimental design, and data analysis, typically supported by a relevant bachelor's or master's degree. Familiarity with lab management software, safety protocols, and equipment maintenance is essential, along with certifications such as CITI or GLP if required. Strong organization, attention to detail, leadership, and communication skills help coordinate team efforts and ensure smooth lab operations. These skills are crucial for maintaining research quality, safety, and productivity in a collaborative scientific environment.

What are some common challenges faced by research assistant lab managers, and how can they be addressed?

Research Assistant Lab Managers often encounter challenges such as balancing administrative duties with hands-on research tasks, maintaining strict laboratory safety protocols, and managing inventory or equipment issues. Effective time management and clear communication with both research staff and principal investigators can help address these challenges. Additionally, staying organized and proactively scheduling regular maintenance or safety checks ensures a smoother workflow and helps prevent disruptions in research activities.

What is the difference between Research Assistant Lab Manager vs Research Assistant?

AspectResearch Assistant Lab ManagerResearch Assistant
CredentialsBachelor's or Master's in relevant field; some managerial experienceBachelor's or Master's in relevant field; no managerial experience typically required
Work EnvironmentLaboratory setting, overseeing lab operationsAssisting with experiments and data collection in labs
ResponsibilitiesManaging lab staff, maintaining equipment, ensuring safety protocolsSupporting research activities, data analysis, preparing reports

The Research Assistant Lab Manager role combines research support with lab management duties, requiring leadership skills and organizational abilities. In contrast, the Research Assistant primarily focuses on assisting with experiments and data collection. Both roles are essential in research settings but differ in scope and responsibilities.

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

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

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

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

Infographic showing various Research Assistant Lab Manager job openings in Wichita, KS as of August 2026, with employment types broken down into 50% Full Time, 17% Temporary, and 33% Contract. Highlights an 84% In-person, and 16% Remote job distribution, with an average salary of $37,675 per year, or $18.1 per hour.

Research Assistant - Wichita, KS

Iterative Health

Wichita, KS

$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.