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Irb Jobs in Kansas (NOW HIRING)

Experience with IRB submissions, study design, data analysis, manuscript development, and journal submission * Experience in rural health, underserved populations, community-based research, or health ...

Familiar with AP Research curriculum and common challenges such as narrowing a viable research question, navigating IRB ethical requirements, and integrating multiple sources into a cohesive ...

AP Research Tutor

Wichita, KS · Remote

$18 - $40/hr

Familiar with AP Research curriculum and common challenges such as narrowing a viable research question, navigating IRB ethical requirements, and integrating multiple sources into a cohesive ...

Clinical Research Coordinator

Wichita, KS · On-site

$21.50 - $28.75/hr

Prepare and submit regulatory documents, including Institutional Review Board (IRB) submissions, continuing reviews, and protocol amendments. * Collaborate with investigators, sponsors, monitors, and ...

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Irb information

See Kansas salary details

$10

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How much do irb jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for irb in Kansas is $33.93, according to ZipRecruiter salary data. Most workers in this role earn between $21.22 and $44.15 per hour, depending on experience, location, and employer.

What is an IRB?

An Institutional Review Board (IRB) is a committee established to review and approve research involving human subjects. The primary purpose of the IRB is to ensure that the rights, welfare, and privacy of participants are protected throughout the research process. IRBs review research proposals to ensure ethical standards are met and that risks to participants are minimized. They are required for most research conducted at universities, hospitals, and other organizations that receive federal funding.

What are the typical responsibilities of an IRB coordinator, and how do they interact with researchers and regulatory bodies?

An IRB (Institutional Review Board) coordinator is responsible for managing the review process of research protocols involving human subjects to ensure compliance with ethical standards and federal regulations. This role involves working closely with researchers to guide them through the submission process, reviewing applications for completeness, and facilitating communication between the IRB committee and research teams. Coordinators also serve as liaisons with regulatory bodies, maintain records, and help organize IRB meetings. Strong organizational, communication, and regulatory knowledge are essential, as coordinators often balance multiple projects and deadlines while ensuring research integrity and participant safety.

What are the key skills and qualifications needed to thrive as an IRB administrator, and why are they important?

To thrive as an IRB Administrator, you need expertise in research ethics, regulatory compliance, and human subject protection, usually supported by a relevant bachelor's or master's degree. Familiarity with IRB management software, federal regulations (such as the Common Rule), and certifications like CIP (Certified IRB Professional) are typically required. Strong organizational skills, attention to detail, and effective communication are crucial for coordinating reviews and guiding researchers. These skills ensure ethical research practices, regulatory compliance, and the protection of research participants.

What is the difference between Irb vs Clinical Research Coordinator?

AspectIrbClinical Research Coordinator
Required CredentialsOften requires IRB training, ethics certificationRequires research experience, sometimes certifications
Work EnvironmentReview boards, research institutionsClinical sites, hospitals, research centers
Employer & Industry UsageUsed in research oversight, ethics reviewUsed in managing clinical trials, patient coordination
Common Search & Comparison IntentUnderstanding roles in research ethicsUnderstanding clinical trial management

IRBs (Institutional Review Boards) focus on ethical review and approval of research protocols, ensuring participant safety. Clinical Research Coordinators manage the day-to-day operations of clinical trials, including patient recruitment and data collection. While both roles are integral to clinical research, IRBs oversee ethical compliance, whereas Coordinators handle trial execution.

How to get an IRB job?

To get an IRB (Institutional Review Board) job, candidates typically need a background in research ethics, healthcare, or related fields, along with relevant experience. Certifications such as the CITI Program Human Subjects Research course are often required, and strong knowledge of federal regulations like 45 CFR 46 is beneficial. Positions may involve reviewing research protocols to ensure ethical standards are met and often require attention to detail and good communication skills.

What does an IRB analyst do?

An IRB analyst reviews research protocols to ensure they comply with ethical standards and regulatory requirements. They evaluate risks, consent processes, and study procedures, often working with institutional review boards to approve or modify research proposals. Strong attention to detail and knowledge of federal regulations are essential for this role.

What are the most commonly searched types of Irb jobs in Kansas?

The most popular types of Irb jobs in Kansas are:

What are popular job titles related to Irb jobs in Kansas?

For Irb jobs in Kansas, the most frequently searched job titles are:

What cities in Kansas are hiring for Irb jobs?

Cities in Kansas with the most Irb job openings:

Infographic showing various Irb job openings in Kansas as of August 2026, with employment types broken down into 83% Full Time, 14% Part Time, 2% Temporary, and 1% Contract. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $70,567 per year, or $33.9 per hour.

Registered Nurse Clinical Research

Overland Park, KS • On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 days ago


Job description

Do you want to join an organization that invests in you as a Registered Nurse Clinical Research? At Kansas City Card Arrhythmia Research, you come first. HCA Healthcare has committed up to $300 million in programs to support our incredible team members over the course of three years.

Responsible for assessing proposed study protocols and for the coordination and implementation of all nursing and administrative activities related to clinical trials. Performs within the parameters for which he or she is qualified by education, training, experience and licensure.

· Coordinates all research study activities with the Principal Investigator and has direct nursing care responsibilities.

· Coordinates and manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical Practices and IRB requirements.

· Develops tactical study procedures.  Develops any necessary study documents not provided by sponsor or IRB

· Educates HCA staff regarding research and study protocols

· Screens and recruits patients based on protocol criteria

· Explains study protocols, procedures and treatments to patients and families. Conducts the Informed Consent process in conjunction with study investigators

· Ensure that an original copy of any subjects Informed Consent Document is the in the research binders, as well as, a copy on the subject's medical record.

· May function as Primary Coordinator for research studies

· Responsible for all investigational drug accountability and dispensing

· Coordinates with Pharmacist if on Delegation Log. Administers Investigational Drug as per protocol

· Serve as a resource for department members for medical interpretations of research process and protocol specifics

· Assess each proposed study protocol with critical analysis of potential implementation and patient care

· Dedicate to creative/innovative growth of research in the division

· Acquire continuing education pertinent to research and applicable licensed profession

· Responsible for maintaining good clinical practice standards, addressing non-compliance issues, developing corrective action plans

· Execute medical orders within parameters of education, training and licensure

· Conduct study activities helping to ensure all safety parameters

· Investigational device accounting and dispensing

· Facilitate administrative review and approval of proposed studies

· Provide/coordinate the highest level of contact, counseling and support services

· Coordinate study activities and patient care with medical staff (cardiologist and PCP, etc.)

· Implement and adhere to study protocol  Perform Phlebotomy and IV procedures

· Prepare laboratory specimens for analysis, monitoring tests and procedures, shipping frozen specimens

· Maintain patient records in EMR and appropriate hospital records

· Assess and report adverse study events, included to the IRB and any research sponsors

· Complete all paperwork affiliated with the study, including but not limited to the requirements of the facility, the IRB and the study Sponsor

· Maintain copies of all research related correspondence

· Conduct study activities helping to ensure all safety parameters

· Maintain professional relationships with sponsors, Clinical Research Organizations, research teams, pharmacies, laboratories, IRB’s, and hospitals for the coordination of research activities

· Review research and pertinent journals, abstracts and scientific literature

EDUCATION AND EXPERIENCE

· Graduate of an accredited school of nursing or other health related field – required with a minimum of two years’ experience in area of research specialty required.

· Minimum of two years clinical research experience.

· Licensed RN/CCRC is preferred/BLS Certification/ACLS preferred

    · Actively maintained CCRC (Certified Clinical Research Coordinator) preferred

    Benefits

    Kansas City Card Arrhythmia Research, offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include:

    • Comprehensive benefits for medical, prescription drug, dental, vision, behavioral health and telemedicine services
    • Wellbeing support, including free counseling and referral services
    • Time away from work programs for paid time off, paid family leave, long- and short-term disability coverage and leaves of absence
    • Savings and retirement resources, including a 401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service), Employee Stock Purchase Plan, flexible spending accounts, preferred banking partnerships, retirement readiness tools, rollover support and financial wellbeing counseling
    • Education support through tuition assistance, student loan assistance, certification support, dependent scholarships and a partnership with Galen College of Nursing
    • Additional benefits for fertility and family building, adoption assistance, life insurance, supplemental health protection plans, auto and home insurance, legal counseling, identity theft protection and consumer discounts

    Learn more about Employee Benefits

    Note: Eligibility for benefits may vary by location.

    Supporting HCA Healthcare's 186 hospitals and 2,400+ sites of care, Physician Services plays a crucial role as the main entry point for patients looking for high-quality healthcare within the HCA Healthcare system. With a focus on meeting the needs of our patients at all access points, Physician Services is dedicated to implementing innovative, physician-driven, value-added solutions to assist physicians in providing high-quality, patient-centered care, aligning with our mission to care for and enhance human life.

    HCA Healthcare has been recognized as one of the World’s Most Ethical Companies® by the Ethisphere Institute more than ten times.  In recent years, HCA Healthcare spent an estimated $3.7 billion in costs for the delivery of charitable care, uninsured discounts, and other uncompensated expenses.


    "Good people beget good people."- Dr. Thomas Frist, Sr.
    HCA Healthcare Co-Founder

    We are a family 270,000 dedicated professionals! Our Talent Acquisition team is reviewing applications for our Registered Nurse Clinical Research opening. Qualified candidates will be contacted for interviews. Submit your resume today to join our community of caring!

    We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.