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 · ...
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 · ...
Clinical Research Coordinator 1 - Pediatrics
Arma, KS · On-site
$18.75 - $25/hr
Understands the IRB submission and review process and when and how to apply for IRB review, including facilitation of study initiation through meticulous and timely preparation of IRB submissions ...
Clinical Research Coordinator 1 - Pediatrics
Arma, KS · On-site
$18.75 - $25/hr
Understands the IRB submission and review process and when and how to apply for IRB review, including facilitation of study initiation through meticulous and timely preparation of IRB submissions ...
Clinical Research Coordinator 1 - Pediatrics
Arma, KS · On-site
$50K - $65K/yr
Understands the IRB submission and review process, and when and how to apply for IRB review, including facilitation of study initiation through meticulous and timely preparation of IRB submissions ...
Clinical Research Coordinator 1 - Pediatrics
Arma, KS · On-site
$50K - $65K/yr
Understands the IRB submission and review process, and when and how to apply for IRB review, including facilitation of study initiation through meticulous and timely preparation of IRB submissions ...
Clinical Research Coordinator 2 - Pediatrics
Arma, KS · On-site
$18.75 - $25/hr
Understand the IRB submission and review process and when and how to apply for IRB review, including facilitation of study initiation through meticulous and timely preparation of IRB submissions ...
Clinical Research Coordinator 2 - Pediatrics
Arma, KS · On-site
$18.75 - $25/hr
Understand the IRB submission and review process and when and how to apply for IRB review, including facilitation of study initiation through meticulous and timely preparation of IRB submissions ...
Senior Clinical Research Coordinator - Pediatrics
Kansas City, KS · On-site
$23.50 - $31/hr
This role ensures compliance with FDA regulations, GCP guidelines, IRB approvals, and HIPAA requirements while supporting study start-up, maintenance, and close-out activities. The SCRC collaborates ...
Senior Clinical Research Coordinator - Pediatrics
Kansas City, KS · On-site
$23.50 - $31/hr
This role ensures compliance with FDA regulations, GCP guidelines, IRB approvals, and HIPAA requirements while supporting study start-up, maintenance, and close-out activities. The SCRC collaborates ...
Nurse Practitioner
Wichita, KS · On-site
Familiarity with delegation-of-authority logs, GCP, IRB processes, and FDA regulatory requirements * CCRP, CCRC, or similar clinical research certification (or willingness to obtain) * Comfort ...
Quick apply
Nurse Practitioner
Wichita, KS · On-site
Familiarity with delegation-of-authority logs, GCP, IRB processes, and FDA regulatory requirements * CCRP, CCRC, or similar clinical research certification (or willingness to obtain) * Comfort ...
Assistant Professor of Research
Wichita, KS · On-site
Experience with IRB submissions, study design, data analysis, manuscript development, and journal submission * Experience in rural health, underserved populations, community-based research, or health ...
Assistant Professor of Research
Wichita, KS · On-site
Experience with IRB submissions, study design, data analysis, manuscript development, and journal submission * Experience in rural health, underserved populations, community-based research, or health ...
This individual will support study-start up activities including IRB/Ancillary committee submissions, and maintenance of regulatory records throughout the life project for assigned cost centers. Job ...
This individual will support study-start up activities including IRB/Ancillary committee submissions, and maintenance of regulatory records throughout the life project for assigned cost centers. Job ...
Senior Clinical Research Coordinator - Pediatrics
Kansas City, KS · On-site
$23.50 - $31/hr
This role ensures compliance with FDA regulations, GCP guidelines, IRB approvals, and HIPAA requirements while supporting study start-up, maintenance, and close-out activities. The SCRC collaborates ...
Senior Clinical Research Coordinator - Pediatrics
Kansas City, KS · On-site
$23.50 - $31/hr
This role ensures compliance with FDA regulations, GCP guidelines, IRB approvals, and HIPAA requirements while supporting study start-up, maintenance, and close-out activities. The SCRC collaborates ...
Research Assistant - Neurology
Kansas City, KS · On-site
$22.88 - $33.17/hr
Maintain IRB compliance, including protocol amendments, progress reports, and regulatory submissions. * Oversee participant recruitment, screening, and informed consent processes. * Coordinate study ...
Research Assistant - Neurology
Kansas City, KS · On-site
$22.88 - $33.17/hr
Maintain IRB compliance, including protocol amendments, progress reports, and regulatory submissions. * Oversee participant recruitment, screening, and informed consent processes. * Coordinate study ...
Assistant Professor of Research
Wichita, KS · On-site
Experience with IRB submissions, study design, data analysis, manuscript development, and journal submission * Experience in rural health, underserved populations, community-based research, or health ...
Assistant Professor of Research
Wichita, KS · On-site
Experience with IRB submissions, study design, data analysis, manuscript development, and journal submission * Experience in rural health, underserved populations, community-based research, or health ...
Nurse Practitioner
Wichita, KS · On-site
Familiarity with delegation-of-authority logs, GCP, IRB processes, and FDA regulatory requirements * CCRP, CCRC, or similar clinical research certification (or willingness to obtain) * Comfort ...
Quick apply
Nurse Practitioner
Wichita, KS · On-site
Familiarity with delegation-of-authority logs, GCP, IRB processes, and FDA regulatory requirements * CCRP, CCRC, or similar clinical research certification (or willingness to obtain) * Comfort ...
Assistant Professor of Research
Wichita, KS · On-site
Experience with IRB submissions, study design, data analysis, manuscript development, and journal submission * Experience in rural health, underserved populations, community-based research, or health ...
Assistant Professor of Research
Wichita, KS · On-site
Experience with IRB submissions, study design, data analysis, manuscript development, and journal submission * Experience in rural health, underserved populations, community-based research, or health ...
Clinical Research Assistant - Internal Medicine (Pulmonary, Critical Care, and Sleep Medicine)
Kansas City, KS · On-site
Experience with research protocols, IRB regulations, and data entry procedures. * Experience with electronic data capture systems (e.g., REDCap, Epic). Skills * Computer skills * Organization
Clinical Research Assistant - Internal Medicine (Pulmonary, Critical Care, and Sleep Medicine)
Kansas City, KS · On-site
Experience with research protocols, IRB regulations, and data entry procedures. * Experience with electronic data capture systems (e.g., REDCap, Epic). Skills * Computer skills * Organization
Research Professional
Harper, KS · On-site
Proofreads and edits citations of research reports, working papers, IRB protocols, and publications. * Maintains effective communication with all members of the faculty and outside institutions.
Research Professional
Harper, KS · On-site
Proofreads and edits citations of research reports, working papers, IRB protocols, and publications. * Maintains effective communication with all members of the faculty and outside institutions.
Clinical Research Assistant - Internal Medicine (Pulmonary, Critical Care, and Sleep Medicine)
Kansas City, KS · On-site
Experience with research protocols, IRB regulations, and data entry procedures. * Experience with electronic data capture systems (e.g., REDCap, Epic). Skills * Computer skills * Organization
Clinical Research Assistant - Internal Medicine (Pulmonary, Critical Care, and Sleep Medicine)
Kansas City, KS · On-site
Experience with research protocols, IRB regulations, and data entry procedures. * Experience with electronic data capture systems (e.g., REDCap, Epic). Skills * Computer skills * Organization
KS · On-site
... IRB) Monitor study medications, laboratory testing, specimen processing, and protocol compliance Assist with policy development, nursing education, and implementation of research protocols Join one ...
KS · On-site
... IRB) Monitor study medications, laboratory testing, specimen processing, and protocol compliance Assist with policy development, nursing education, and implementation of research protocols Join one ...
Collaborate with DPRR and SnapIT's program and knowledge‑management staff to support institutional approvals and compliance documentation (e.g., ARMD, OMB, IRB, AHRPO submissions). * Provide ...
Quick apply
Collaborate with DPRR and SnapIT's program and knowledge‑management staff to support institutional approvals and compliance documentation (e.g., ARMD, OMB, IRB, AHRPO submissions). * Provide ...
AP Research Tutor
Overland Park, 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 ...
AP Research Tutor
Overland Park, 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 ...
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 ...
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 ...
Irb information
See Kansas salary details
$10.82 - $16.34
13% of jobs
$20.31 is the 25th percentile. Wages below this are outliers.
$16.34 - $21.86
17% of jobs
$21.86 - $27.38
15% of jobs
The median wage is $28.40 / hr.
$27.38 - $32.90
29% of jobs
$33.93 is the 75th percentile. Wages above this are outliers.
$32.90 - $38.42
9% of jobs
$38.42 - $43.94
2% of jobs
$43.94 - $49.45
7% of jobs
$49.45 - $54.97
7% of jobs
$54.97 - $60.49
1% of jobs
$60.49 - $66.01
0% of jobs
$66.01 - $71.53
0% of jobs
$10
$33
$71
How much do irb jobs pay per hour?
What is the job of the IRB?
What are the key skills and qualifications needed to thrive as an IRB (Institutional Review Board) Administrator, and why are they important?
What are the typical responsibilities of an IRB coordinator, and how do they interact with researchers and regulatory bodies?
What is an IRB?
How much do IRB members make?
How to get a job on an IRB?
What jobs pay 4000 a week without a degree?
What is the difference between Irb vs Clinical Research Coordinator?
| Aspect | Irb | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Often requires IRB training, ethics certification | Requires research experience, sometimes certifications |
| Work Environment | Review boards, research institutions | Clinical sites, hospitals, research centers |
| Employer & Industry Usage | Used in research oversight, ethics review | Used in managing clinical trials, patient coordination |
| Common Search & Comparison Intent | Understanding roles in research ethics | Understanding 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.

Other
Medical, Dental, Vision, Life, Retirement, PTO
Posted 9 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
BenefitsKansas 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.