Responsibilities include (but are not limited to) the following: 1) Assist with development and implementation of human research protection for all NTR IRB partners; 2) Perform comprehensive ...
Responsibilities include (but are not limited to) the following: 1) Assist with development and implementation of human research protection for all NTR IRB partners; 2) Perform comprehensive ...
Responsibilities include (but are not limited to) the following: 1) Assist with development and implementation of human research protection for all NTR IRB partners; 2) Perform comprehensive ...
Responsibilities include (but are not limited to) the following: 1) Assist with development and implementation of human research protection for all NTR IRB partners; 2) Perform comprehensive ...
Responsibilities include (but are not limited to) the following: 1) Assist with development and implementation of human research protection for all NTR IRB partners; 2) Perform comprehensive ...
Responsibilities include (but are not limited to) the following: 1) Assist with development and implementation of human research protection for all NTR IRB partners; 2) Perform comprehensive ...
Responsibilities include (but are not limited to) the following: 1) Assist with development and implementation of human research protection for all NTR IRB partners; 2) Perform comprehensive ...
Responsibilities include (but are not limited to) the following: 1) Assist with development and implementation of human research protection for all NTR IRB partners; 2) Perform comprehensive ...
Clinical Research Assistant B
Center, TX ยท On-site
$19.47 - $19.81/hr
Posted Job Title Clinical Research Assistant B Job Profile Title Clinical Research Assistant B ... IRB Maintains telephone follow-up with all study patients as dictated by protocol in a timely ...
Clinical Research Assistant B
Center, TX ยท On-site
$19.47 - $19.81/hr
Posted Job Title Clinical Research Assistant B Job Profile Title Clinical Research Assistant B ... IRB Maintains telephone follow-up with all study patients as dictated by protocol in a timely ...
Clinical Research Assistant B
$19.47 - $19.81/hr
Posted Job Title Clinical Research Assistant B Job Profile Title Clinical Research Assistant B ... IRB Maintains telephone follow-up with all study patients as dictated by protocol in a timely ...
Clinical Research Assistant B
$19.47 - $19.81/hr
Posted Job Title Clinical Research Assistant B Job Profile Title Clinical Research Assistant B ... IRB Maintains telephone follow-up with all study patients as dictated by protocol in a timely ...
Physician Assistant (Associate) - Clinical Research
Mckinney, TX ยท On-site
$92K - $125K/yr
Physician Assistant (Associate) Opportunity Unique opportunity to make an impact in the healthcare ... the IRB-approved plan, sponsor requirements, and organizational procedures. This role does not ...
Physician Assistant (Associate) - Clinical Research
Mckinney, TX ยท On-site
$92K - $125K/yr
Physician Assistant (Associate) Opportunity Unique opportunity to make an impact in the healthcare ... the IRB-approved plan, sponsor requirements, and organizational procedures. This role does not ...
Physician Assistant (Associate) - Clinical Research
Mckinney, TX ยท On-site
$87K - $117K/yr
We are seeking a Physician Assistant (Associate) to join our established team. Someone with a ... the IRB-approved plan, sponsor requirements, and organizational procedures. This role does not ...
Quick apply
Physician Assistant (Associate) - Clinical Research
Mckinney, TX ยท On-site
$87K - $117K/yr
We are seeking a Physician Assistant (Associate) to join our established team. Someone with a ... the IRB-approved plan, sponsor requirements, and organizational procedures. This role does not ...
Job Title RSSI Graduate Research Assistant Agency Texas A&M Agrilife Extension Service Department 4 ... Understanding of IRB protocols and application procedures * Excellent interpersonal relationship ...
Job Title RSSI Graduate Research Assistant Agency Texas A&M Agrilife Extension Service Department 4 ... Understanding of IRB protocols and application procedures * Excellent interpersonal relationship ...
Job Title RSSI Graduate Research Assistant Agency Texas A&M Agrilife Extension Service Department 4 ... Understanding of IRB protocols and application procedures * Excellent interpersonal relationship ...
Job Title RSSI Graduate Research Assistant Agency Texas A&M Agrilife Extension Service Department 4 ... Understanding of IRB protocols and application procedures * Excellent interpersonal relationship ...
Sub l /Nurse Practitioner
San Antonio, TX ยท On-site
Planning and Management * Assist in recruitment of additional research studies, especially through ... Provide the sponsor and IRB with documentation of credentials as requested. * Demonstrate the ...
Sub l /Nurse Practitioner
San Antonio, TX ยท On-site
Planning and Management * Assist in recruitment of additional research studies, especially through ... Provide the sponsor and IRB with documentation of credentials as requested. * Demonstrate the ...
Sub l /Nurse Practitioner
San Antonio, TX ยท On-site
Planning and Management * Assist in recruitment of additional research studies, especially through ... Provide the sponsor and IRB with documentation of credentials as requested. * Demonstrate the ...
Sub l /Nurse Practitioner
San Antonio, TX ยท On-site
Planning and Management * Assist in recruitment of additional research studies, especially through ... Provide the sponsor and IRB with documentation of credentials as requested. * Demonstrate the ...
Graduate Research Assistant
Austin, TX ยท On-site
Graduate Research Assistant ---- Hiring Department: Population Research Center ---- Position Open ... Willingness to complete required training and follow lab protocols for secure, ethical, and IRB ...
Graduate Research Assistant
Austin, TX ยท On-site
Graduate Research Assistant ---- Hiring Department: Population Research Center ---- Position Open ... Willingness to complete required training and follow lab protocols for secure, ethical, and IRB ...
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Regulatory Specialist (Clinical Research)
Pearland, TX ยท On-site
$58K - $65K/yr
IRB & Regulatory Submissions * Prepare and submit IRB applications, continuing reviews, amendments ... Maintain ongoing inspection readiness of regulatory files. * Assist with compilation of regulatory ...
Quick apply
Be Seen First
Regulatory Specialist (Clinical Research)
Pearland, TX ยท On-site
$58K - $65K/yr
IRB & Regulatory Submissions * Prepare and submit IRB applications, continuing reviews, amendments ... Maintain ongoing inspection readiness of regulatory files. * Assist with compilation of regulatory ...
... 99 hours per week. * Assist in the coordination and monitoring of all research activities ... May prepare IRB documents under the direction of the Principal Investigator and assists with ...
... 99 hours per week. * Assist in the coordination and monitoring of all research activities ... May prepare IRB documents under the direction of the Principal Investigator and assists with ...
Research Assistant
$18.25 - $25.25/hr
Sponsor-provided and IRB-approved protocol * All amendments * Investigator Brochure * Sponsor ... Medical Assistant Certification preferred Knowledge amp; Skills: * Knowledge of medical terminology ...
Research Assistant
$18.25 - $25.25/hr
Sponsor-provided and IRB-approved protocol * All amendments * Investigator Brochure * Sponsor ... Medical Assistant Certification preferred Knowledge amp; Skills: * Knowledge of medical terminology ...
... 99 hours per week. * Assist in the coordination and monitoring of all research activities ... May prepare IRB documents under the direction of the Principal Investigator and assists with ...
... 99 hours per week. * Assist in the coordination and monitoring of all research activities ... May prepare IRB documents under the direction of the Principal Investigator and assists with ...
... 99 hours per week. * Assist in the coordination and monitoring of all research activities ... May prepare IRB documents under the direction of the Principal Investigator and assists with ...
... 99 hours per week. * Assist in the coordination and monitoring of all research activities ... May prepare IRB documents under the direction of the Principal Investigator and assists with ...
Clinical Trial Research Assistant
The Woodlands, TX ยท On-site
$15 - $18/hr
Clinical Trial Research Assistant The Woodlands, TX | Full-Time | Private Outpatient Medical Clinic ... Support the preparation and submission of reports to regulatory bodies (IRB, FDA, DSMB). * Maintain ...
Quick apply
Clinical Trial Research Assistant
The Woodlands, TX ยท On-site
$15 - $18/hr
Clinical Trial Research Assistant The Woodlands, TX | Full-Time | Private Outpatient Medical Clinic ... Support the preparation and submission of reports to regulatory bodies (IRB, FDA, DSMB). * Maintain ...
Research Assistant I (Lab) (4170)
$18.25 - $25/hr
Sponsor-provided and IRB-approved protocol * All amendments * Investigator Brochure * Sponsor ... Medical Assistant Certification preferred Knowledge & Skills: * Knowledge of medical terminology ...
Research Assistant I (Lab) (4170)
$18.25 - $25/hr
Sponsor-provided and IRB-approved protocol * All amendments * Investigator Brochure * Sponsor ... Medical Assistant Certification preferred Knowledge & Skills: * Knowledge of medical terminology ...
Irb Assistant information
What is an IRB assistant?
What skills and qualifications are needed to thrive as an IRB assistant?
What are common challenges faced by an IRB assistant and how can they be managed?
What is the difference between Irb Assistant vs Clinical Research Coordinator?
| Aspect | Irb Assistant | Clinical Research Coordinator |
|---|---|---|
| Credentials | High school diploma or associate's; some roles may require certification | Bachelor's degree often preferred; certifications like CCRP beneficial |
| Work Environment | Office and clinical settings, supporting IRB processes | Clinical sites, hospitals, or research centers managing studies |
| Employer & Industry | Research institutions, hospitals, universities | Pharmaceutical companies, research organizations, hospitals |
| Job Focus | Assisting with IRB submissions, documentation, compliance | Overseeing study coordination, patient recruitment, data collection |
The Irb Assistant primarily supports IRB-related tasks such as documentation and compliance, often requiring less extensive education. In contrast, a Clinical Research Coordinator manages the overall conduct of clinical trials, including patient interactions and data management. Both roles are essential in research but differ in scope and responsibilities.
What are the most commonly searched types of Irb jobs in Texas?
The most popular types of Irb jobs in Texas are:
What are popular job titles related to Irb Assistant jobs in Texas?
For Irb Assistant jobs in Texas, the most frequently searched job titles are:
- Entry Level Clinical Research Nurse
- Work From Home Velocity Clinical Research
- Hourly Clinical Research Protocol Writer
- Nyu Langone Research Assistant
- Entry Level Researcher
- Internship Clinical Research Assistant Volunteer
- Law School Research Assistant
- Nextstage Clinical Research Llc
- Alien Research
- Internship Clinical Psychology Research Assistant
What job categories do people searching Irb Assistant jobs in Texas look for?
The top searched job categories for Irb Assistant jobs in Texas are:
- Transportation Research Assistant
- Research Psychiatric Center
- Volunteer Medical Device Clinical Research
- Research Demography
- Emergency Medicine Research Assistant
- Part Time Research Assistant
- Undergrad Research Assistant
- Seasonal Senior Clinical Research Associate
- Full Time Cvs Research
- Online Research Assistant
What cities in Texas are hiring for Irb Assistant jobs?
Cities in Texas with the most Irb Assistant job openings:

Institutional Review Board Compliance Manager
Fort Worth, TX โข On-site
Full-time
Re-posted 8 days ago
Job description
Job no: 514161
Work type: Staff
Location: Fort Worth
Categories: Compliance
Title: Institutional Review Board Compliance Manager
Employee Classification: Compliance Manager
Campus: University of North Texas - Health Science Center
Division: HSC-Div of Rsrch & Innovation
SubDivision-Department: HSC-Div of Rsrch & Innovation
Department: HSC-Rsrch Compliance-390000
Job Location: Fort Worth
Salary: Commensurate With Experience
FTE: 1.000000
Retirement Eligibility: TRS Eligible
About Us - Values Overview
Welcome to the University of North Texas System. The UNT System includes the University of North Texas in Denton and Frisco, the University of North Texas at Dallas and UNT Dallas College of Law, and University of North Texas Health Fort Worth. We are the only university system based exclusively in the robust Dallas-Fort Worth region. We are growing with the North Texas region, employing more than 14,000 employees, educating a record 49,000+ students across our system, and awarding nearly 12,000 degrees each year.
We are one team comprised of individuals who are committed to excellence, curiosity and innovation. We are transforming lives and creating economic opportunity through education. We champion a people-first values-based culture where We Care about each other and those we serve. We believe that we are Better Together because we foster an environment of respect, belonging, and access for all. We demonstrate Courageous Integrity through setting exceptional standards and acting in the best interest of our communities. We are encouraged to Be Curious about opportunities for learning, creating, discovering, and innovating, and are encouraged to learn from failure. Show Your Fire by joining our team and exhibiting your passion and pride in your work as part of our UNT System team.
Learn more about the UNT System and how we live our values at www.UNTSystem.edu.
Department Summary
The Office of Research Compliance (ORC) at the University of North Texas Health Science Center is located within the Division of Research & Innovation (DRI). The ORC works with offices responsible for specific components of research compliance and university research oversight committees such as the Institutional Review Board, Institutional Biosafety, Institutional Animal Care and Use, Research Conflict of Interest committees and the Export Control/Research Security/International Compliance Office to ensure the responsible conduct of research and compliance with university policies and federal regulations related to research activity. The office oversees development and implementation of policies, procedures, and educational activities which satisfy university policies, state, and federal regulations governing the conduct of research. The ORC is responsible for monitoring regulatory updates and making recommendations to the university to ensure compliance.
Position Overview
The Office of Research Compliance (ORC) at the University of North Texas Health Science Center, in conjunction with the North Texas Regional Institutional Review Board (NTR IRB), is seeking to hire an IRB Compliance Manager to join our team. This position will report directly to the Director of the NTR IRB and will also work closely with the ORC. Responsibilities include (but are not limited to) the following: 1) Assist with development and implementation of human research protection for all NTR IRB partners; 2) Perform comprehensive administrative and regulatory reviews of designated IRB submissions (which include biomedical, clinical trial, and social/behavioral science studies) by ensuring applications/submissions meet all federal agency regulatory requirements for human subject research; 3) Assist with ongoing education and training for all affiliated researchers to ensure appropriate compliance with federal, state and university/institutional policies and regulations associated with human subject research; 4) Prepare documents for review by the IRB reviewers/committee; 5) Assist with oversight, attendance and coordination of IRB committee meetings and communicate outcomes to investigators, relevant institutional officials, and federal agencies (when needed); 6) Assist with development and roll out of inhouse compliance training programs, workshops, seminars, guidance documents and other outreach and educational tools and training related to IRB and human subject research; 7) Assist in the daily activities, accreditation efforts, special projects and operation of the NTR IRB.
Minimum Qualifications
Bachelor's degree and four (4) years related experience; or equivalent combination of education and experience.
Knowledge, Skills and Abilities
- 1) Thorough knowledge of appropriate federal regulatory agencies (FDA, OHRP);
- 2) Skill set in development and update of web sites, web pages and online outreach and training tools;
- 3) Well-developed organizational and analytical skills; outstanding attention to detail; and objective observer;
- 4) Exceptionally strong written, verbal, and presentation skills; education and training experience in higher education preferred;
- 5) Highly collaborative and shows initiative; 6) High level of professionalism, maturity, diplomacy, and strict confidentiality.
Preferred Qualifications
The preferred candidate will possess the following additional qualifications:
- Bachelors degree in any health sciences field, Masters Degree preferred;
- 3 years human subject research experience or 3 years in an IRB-related role;
- Certified IRB Professional (CIP) Certification or eligibility for such certification;
- Prior experience with critical thinking, project management, document management and client interactions;
- 1-3 years across all categories in hospital research setting, university, or clinical research operation.
Required License/Registration/Certifications
None
Job Duties
- Assist NTR IRB Director with daily IRB operations, which includes development and implementation of human research protection for all NTR IRB partners (including but not necessarily limited to researchers from UNTHSC, John Peter Smith Health Network and other partners). This position will work directly with researchers/investigators from all organizations (as needed), and will also work closely with the IRB Committee (Chair and Board members) and fellow IRB Compliance Managers.
- Perform comprehensive administrative and regulatory reviews of designated IRB submissions (which include biomedical, clinical trial and social/behavioral science studies) by ensuring applications/submissions meet all federal agency regulatory requirements (e.g., Office for Human Research Protections OHRP; Food and Drug Administration FDA) for human subject research. This includes review of new submissions, in addition to continuing reviews, amendments, reportable events, etc. Additionally, this position will also ensure all institutional policies/procedures regarding human subject research are met, in addition to any other state and local regulations/policies.
- Assist with ongoing education and training for all researchers/investigators to ensure appropriate compliance with federal, state, and university/institutional policies and regulations associated with human subject research. This includes providing thorough, clear and detailed (education-based) guidance or feedback to researchers/investigators/NTR IRB partners regarding these matters. To this aim, the incumbent is expected to be knowledgeable and stay up-to-date regarding federal, state, and local/institutional regulations/policies/guidance.
- Prepare documents for review by the IRB Committee. This may include (but are not limited to) preparation of comments and pre-review notes for Board Member review, in addition to following up with researchers/investigators on information needed in preparation of discussion at IRB meetings.
- Assist with oversight, attendance and coordination of IRB committee meetings and communicate outcomes to investigators and relevant institutional officials. This also includes (but not be limited to) preparing meeting agendas, setting up/arranging the IRB meetings, tracking attendance/quorum during meetings, and drafting/finalizing detailed meeting minutes (which adhere to all federal regulatory requirements)
- Assist the NTR IRB Director, in addition to the ORC Executive Director, Education Outreach Coordinator and other research supporting units, with development and roll out of in-house compliance training programs, workshops, seminars, guidance documents and other outreach and educational tools and training related to IRB and human subject research. This may include preparation of educational/training documents, training videos, procedure and guidance manuals, or presentations to researchers/investigators, other key stakeholders or NTR IRB partners/clients. Additionally, assist in keeping information on the NTR IRB website appropriately updated.
Physical Requirements
- Repeating motions that may include the wrists, hands and/or fingers.
- Sedentary work that primarily involves sitting/standing.
- Communicating with others to exchange information.
Environmental Hazards
- No adverse environmental conditions expected.
Work Schedule
M-F, 8 AM - 5 PM; eligible hybrid schedule
Driving University Vehicle
No
Security Sensitive
This is a Security Sensitive Position.
Special Instructions
Applicants must submit a minimum of two professional references as part of their application. If needed, additional references can be added after the application has been submitted.
Benefits
For information regarding our Benefits, click here.
EEO Statement
The University of North Texas System is firmly committed to equal opportunity and does not permit -and takes actions to prevent - discrimination, harassment (including sexual violence, domestic violence, dating violence and stalking), and retaliation on the basis of race, color, religion, national origin, sex, age, disability, genetic information, or veteran status in its application, employment practices, and facilities; nor permits race, color, national origin, religion, age, disability, veteran status, or sex discrimination and harassment in its admissions processes, and educational programs and activities. UNT System Administration promptly investigates complaints of discrimination, harassment, and related retaliation and takes remedial action when appropriate. System Administration also takes actions to prevent retaliation against individuals who oppose any form of harassment or discriminatory practice, file a charge or report, or testify, assist, or participate in a related investigation or proceeding.
Advertised: 26 May 2026 Central Daylight Time
Applications close:
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About University of North Texas System
Sourced by ZipRecruiter
Industry
Colleges, universities, and professional schools
Company size
10,000+ Employees
Headquarters location
Dallas, TX, US
Year founded
1890