... 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 ...
... 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 ...
Registered Nurse Clinical Research
Leawood, KS · On-site
$67K - $84K/yr
... 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. • ...
Registered Nurse Clinical Research
Leawood, KS · On-site
$67K - $84K/yr
... 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. • ...
... 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. * Assess each ...
... 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. * Assess each ...
Clinical Research Coordinator 2 - Pediatrics
Arma, KS · On-site
$18.75 - $25/hr
The CRC 2 works under the general direction of the Director of Clinical Research, a principal ... Understand the IRB submission and review process and when and how to apply for IRB review ...
Clinical Research Coordinator 2 - Pediatrics
Arma, KS · On-site
$18.75 - $25/hr
The CRC 2 works under the general direction of the Director of Clinical Research, a principal ... Understand the IRB submission and review process and when and how to apply for IRB review ...
... IRB applications, amendments, informed consent). * Experience with industry sponsored clinical ... Knowledge and ability to provide direct patient care, including aseptic techniques, in a ...
... IRB applications, amendments, informed consent). * Experience with industry sponsored clinical ... Knowledge and ability to provide direct patient care, including aseptic techniques, in a ...
Advanced Endoscopy Technician Full Time Days
Shawnee Mission, KS · On-site
$18.96 - $30.34/hr
Prepares patients for procedures as directed by the registered nurse, participates in the care of ... Understanding IRB rules and processes for research procedures in the hospital setting [Required ...
Advanced Endoscopy Technician Full Time Days
Shawnee Mission, KS · On-site
$18.96 - $30.34/hr
Prepares patients for procedures as directed by the registered nurse, participates in the care of ... Understanding IRB rules and processes for research procedures in the hospital setting [Required ...
Clinical Research Coordinator
Wichita, KS · On-site
$21.75 - $28.75/hr
... IRB reviews. * Support the Project Director, Clinic Coordinator, or PI in the administration of the grant/contract per federal rules and regulations and/or specific grant/contract language.
Clinical Research Coordinator
Wichita, KS · On-site
$21.75 - $28.75/hr
... IRB reviews. * Support the Project Director, Clinic Coordinator, or PI in the administration of the grant/contract per federal rules and regulations and/or specific grant/contract language.
... IRB applications, amendments, informed consent). * Experience with industry sponsored clinical ... Knowledge and ability to provide direct patient care, including aseptic techniques, in a ...
... IRB applications, amendments, informed consent). * Experience with industry sponsored clinical ... Knowledge and ability to provide direct patient care, including aseptic techniques, in a ...
Clinical Research Coordinator
Wichita, KS · On-site
$21.75 - $28.75/hr
... IRB reviews. * Support the Project Director, Clinic Coordinator, or PI in the administration of the grant/contract per federal rules and regulations and/or specific grant/contract language.
Clinical Research Coordinator
Wichita, KS · On-site
$21.75 - $28.75/hr
... IRB reviews. * Support the Project Director, Clinic Coordinator, or PI in the administration of the grant/contract per federal rules and regulations and/or specific grant/contract language.
Medical Assistant
Kansas City, KS · On-site
$44K - $62K/yr
Adherence to Good Clinical Practice (GCP) guidelines, Institutional Review Board (IRB) requirements ... Prepare and administer medications and vaccinations as directed and appropriately delegated by a ...
Medical Assistant
Kansas City, KS · On-site
$44K - $62K/yr
Adherence to Good Clinical Practice (GCP) guidelines, Institutional Review Board (IRB) requirements ... Prepare and administer medications and vaccinations as directed and appropriately delegated by a ...
Medical Assistant
$44K - $62K/yr
Adherence to Good Clinical Practice (GCP) guidelines, Institutional Review Board (IRB) requirements ... Prepare and administer medications and vaccinations as directed and appropriately delegated by a ...
Medical Assistant
$44K - $62K/yr
Adherence to Good Clinical Practice (GCP) guidelines, Institutional Review Board (IRB) requirements ... Prepare and administer medications and vaccinations as directed and appropriately delegated by a ...
Research Assistant - Wichita, KS
Wichita, KS · On-site
$17.25 - $23.75/hr
... IRB requirements. * Assist with screening subjects for eligibility using protocol-specific ... Enter all patient visit data in eCRF and CTMS on a daily basis or as directed. * Arrange secure ...
Quick apply
Research Assistant - Wichita, KS
Wichita, KS · On-site
$17.25 - $23.75/hr
... IRB requirements. * Assist with screening subjects for eligibility using protocol-specific ... Enter all patient visit data in eCRF and CTMS on a daily basis or as directed. * Arrange secure ...
Clinical Research Coordinator II
Lenexa, KS · On-site
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Clinical Research Coordinator II
Lenexa, KS · On-site
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Clinical Research Coordinator II
Lenexa, KS · On-site
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Quick apply
Clinical Research Coordinator II
Lenexa, KS · On-site
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Clinical Research Coordinator II
Lenexa, KS · On-site
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Clinical Research Coordinator II
Lenexa, KS · On-site
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Clinical Research Coordinator II
Lenexa, KS · On-site
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Clinical Research Coordinator II
Lenexa, KS · On-site
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Clinical Research Coordinator II
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Clinical Research Coordinator II
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Clinical Research Coordinator II
Lenexa, KS · On-site
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Quick apply
Clinical Research Coordinator II
Lenexa, KS · On-site
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Clinical Research Coordinator II
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Clinical Research Coordinator II
$27 - $32/hr
This position reports to the Site Manager or Site Director. Key Responsibilities (Essential ... IRB and adverse event reporting * Strong interpersonal skills with attention to detail a must
Clinical Research Nurse Coordinator
$66K - $83K/yr
Coordinate with sponsor, Research Institute, IRB, or FDA as necessary to support studies. * In ... Ability to engage in self-directed education and development * IV therapy skills required * Basic ...
Clinical Research Nurse Coordinator
$66K - $83K/yr
Coordinate with sponsor, Research Institute, IRB, or FDA as necessary to support studies. * In ... Ability to engage in self-directed education and development * IV therapy skills required * Basic ...
Irb Director information
See Kansas salary details
$21.6K - $34.9K
11% of jobs
$34.9K - $48.1K
14% of jobs
$48.5K is the 25th percentile. Wages below this are outliers.
$48.1K - $61.4K
18% of jobs
The median wage is $66.8K / yr.
$61.4K - $74.6K
18% of jobs
$74.6K - $87.9K
7% of jobs
$97.4K is the 75th percentile. Wages above this are outliers.
$87.9K - $101.1K
10% of jobs
$101.1K - $114.3K
9% of jobs
$114.3K - $127.6K
4% of jobs
$127.6K - $140.8K
3% of jobs
$140.8K - $154.1K
4% of jobs
$154.1K - $167.3K
2% of jobs
$21.6K
$80.3K
$167.3K
How much do irb director jobs pay per year?
What is an IRB director?
An IRB (Institutional Review Board) Director oversees the ethical review process for research involving human subjects, ensuring compliance with federal regulations and institutional policies. They manage the IRB office, coordinate board meetings, review protocols, and provide guidance to researchers on ethical issues. The IRB Director also ensures that research projects adhere to ethical standards, maintains documentation, and facilitates training for staff and researchers. Their role is critical in protecting the rights and welfare of human subjects in research.
What are the main responsibilities of an IRB director in a typical week?
As an IRB Director, you can expect to oversee research protocol reviews, ensure adherence to regulatory and ethical standards, and facilitate meetings with board members. Your week may involve providing guidance to investigators, training staff on compliance issues, and coordinating with legal, medical, and research professionals to address complex ethical questions. Many IRB Directors also play a role in policy development and ongoing process improvements. This role requires balancing administrative duties with hands-on oversight to ensure that all human subjects research meets the highest standards of safety and ethics.
What are the key skills and qualifications needed to thrive in the IRB director position, and why are they important?
To thrive as an IRB Director, you need in-depth knowledge of human subjects research regulations, attention to detail, and experience in research ethics, typically supported by an advanced degree in a relevant field. Proficiency with electronic IRB management systems, compliance tracking software, and certification such as CIP (Certified IRB Professional) are commonly required. Outstanding leadership, communication, and problem-solving abilities help IRB Directors effectively manage review panels and address complex ethical considerations. These skills ensure the integrity and compliance of research involving human subjects while fostering a culture of ethical oversight.
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 Director jobs in Kansas?
For Irb Director jobs in Kansas, the most frequently searched job titles are:
What job categories do people searching Irb Director jobs in Kansas look for?
The top searched job categories for Irb Director jobs in Kansas are:

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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
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.