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Full Time Irb Jobs (NOW HIRING)

Allen Spolden

Cath Lab/IRB Technologist

Lewiston, ID · On-site

$2.2K - $3.0K/wk

Job Opportunity Date Opened 04/03/2025 Job Type: Full time Industry: Health Care Work Experience: 1-3 years Salary: 84,000 City: Lewiston State/Province: ID Country: United States Zip/Postal Code ...

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How much do full time irb jobs pay per year?

As of Sep 2, 2026, the average yearly pay for full time irb in the United States is $330,066.00, according to ZipRecruiter salary data. Most workers in this role earn between $311,000.00 and $385,500.00 per year, depending on experience, location, and employer.

What is a full time IRB?

A Full Time IRB (Institutional Review Board) professional is a specialist who works full-time to review, approve, and oversee research involving human subjects to ensure that ethical standards and regulatory requirements are met. They are responsible for protecting the rights and welfare of research participants by conducting ethical reviews, monitoring ongoing research, and providing guidance to researchers. Full Time IRB staff often work in universities, hospitals, or research institutions, and collaborate closely with researchers and compliance officers. Their role is essential to maintaining the integrity and safety of scientific research involving humans.

What are the typical responsibilities of a full time IRB coordinator, and how does the role interact with researchers and regulatory bodies?

A full-time IRB coordinator is responsible for managing the ethical review process of research involving human subjects. This includes reviewing research proposals for compliance with federal regulations, facilitating IRB meetings, communicating required changes to researchers, and maintaining accurate records. Coordinators act as a critical liaison between researchers, IRB members, and regulatory agencies to ensure studies are conducted ethically and participants are protected. Daily tasks often involve document review, correspondence, and providing guidance to investigators, making strong communication and organizational skills essential.

What are the key skills and qualifications needed to thrive as a full time IRB professional, and why are they important?

To thrive as a full-time IRB professional, you need a comprehensive understanding of research ethics, regulatory compliance (such as 45 CFR 46 and FDA regulations), and typically a background in life sciences or healthcare. Familiarity with electronic IRB management systems, compliance databases, and certifications like CIP (Certified IRB Professional) are commonly required. Strong analytical thinking, attention to detail, and effective communication are essential soft skills for reviewing protocols and collaborating with researchers. These competencies are critical for ensuring the protection of human research subjects and maintaining institutional and federal compliance.

What is the difference between Full Time Irb vs Part Time Irb?

AspectFull Time IrbPart Time Irb
CredentialsIRB certification, research ethics trainingIRB certification, research ethics training
Work EnvironmentOffice, research institutions, hospitalsFlexible, part-time settings, remote options
Employer & IndustryResearch institutions, hospitals, universitiesResearch organizations, academic institutions
Work Hours40+ hours/weekLess than 20 hours/week

Full Time Irb roles typically involve a standard 40+ hour workweek, requiring full-time commitment and consistent presence in research settings. Part Time Irb positions offer flexible hours, often less than 20 hours weekly, suitable for those balancing other responsibilities. Both roles require IRB certification and knowledge of research ethics, but the main difference lies in hours and work setting.

How to become a full time IRB?

To become a full-time IRB (Institutional Review Board) member, individuals typically need a background in research, ethics, or related fields, along with experience in human subjects research. Certification in research ethics or compliance, such as CITI Program training, is often required, and strong analytical and communication skills are essential for reviewing research protocols. Full-time IRB roles may also require familiarity with federal regulations like the Common Rule and institutional policies.
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Full Time Irb jobs near you
Infographic showing various Full Time Irb job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $330,066 per year, or $158.7 per hour.

Research Regulatory Coordinator

Arkansas Childrens Hospital

Little Rock, AR • On-site

Full-time

Posted 8 days ago

Arkansas Children's Hospital rating

7.5

Company rating: 7.5 out of 10

Based on 58 frontline employees who took The Breakroom Quiz

298th of 1,064 rated hospitals

Job description

ARKANSAS CHILDREN'S IS A TOBACCO FREE WORKPLACE. FLU VACCINES ARE REQUIRED. ARKANSAS CHILDREN'S IS AN EQUAL OPPORTUNITY EMPLOYER. ALL QUALIFIED APPLICANTS WILL RECEIVE CONSIDERATION FOR EMPLOYMENT WITHOUT REGARD TO RACE, COLOR, RELIGION, SEX, SEXUAL ORIENTATION, GENDER IDENTITY OR EXPRESSION, NATIONAL ORIGIN, AGE, DISABILITY, PROTECTED VETERAN STATUS OR ANY OTHER CHARACTERISTIC PROTECTED BY FEDERAL, STATE, OR LOCAL LAWS.

CURRENT EMPLOYEES: Please apply via the internal career site by logging into your Workday Account (https://www.myworkday.com/archildrens/)and search the "Find Jobs" report.

Work Shift:

Please see job description for details.

Time Type:

Full time

Department:

CC035772 Regulatory Clinical Research OperationsSummary:This position will oversee all regulatory affairs business for researchers within Arkansas Children's Research Institute. This individual will support researchers ensuring that research protocols involving human subjects abide by the federal regulation, state codes, IRB oversight standard, and the institutional policies governing human subjects research.Additional Information:

This position will oversee all regulatory affairs business for researchers within Arkansas Children's Research Institute. This individual will support researchers ensuring that research protocols involving human subjects abide by the federal regulation, state codes, IRB oversight standard, and the institutional policies governing human subjects research.

Required Education:High school diploma or GED or equivalentRecommended Education:Bachelor's degree in a related field of study.Required Work Experience:High School Diploma/GED, or 2 years of experience in lieu of a diploma/GED.Recommended Work Experience:Required Certifications:Recommended Certifications:Certified Clinical Research Professional (CCRP) - Society of Clinical Research AssociatesDescription

1. Prepares and submits IRB documents under the direction of the PI/Research Administrator and prepares regulatory documents to be sent to the Sponsor. Assists with submitting documents and contracts through regulatory and IRB processes and approval; may draft various communications with Sponsor.

2. Performs high quality review of start-up regulatory forms and associated documentation prior to submission to sponsor, IRB and filing in Regulatory Binders, to assure documents meet all site and sponsor requirements.

3. Coordinates and participates in the pre-site and, site initiation visits and Interim Monitoring Visits as required per protocol. Planning and design of source documents for protocols.

4. Manages and proofreads updated study regulatory drafts to ensure the accuracy and completeness of changes. Utilizes data resources external to research area, as well as develops and facilitates productive working relationship with the study monitors.

5. Compliance with all Office of Compliance, and any other departmental training requirements.

6. Communicate to researchers and research team members review board decisions or compliance issues which may negatively impact the future of their research protocols.

7. Negotiate revisions with researchers and sponsors to facilitate research review board consideration and approval to ensure regulatory compliance. (Understand the IRB's operational requirements)

8. Communicate to researchers and research team members review board decisions or compliance issues which may negatively impact the future of their research protocols. Monitor compliance of research investigators as to provisions and directions given by the review board regarding research protocols

9. Attends and participates in conferences which support the objectives and goals of the specific protocols.
b. Actively participates in study related meetings.
c. Participates in educational programs and professional activities to gain knowledge of current trends, practices and developments.

10. Performs other duties as assigned.

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