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Full Time Irb Jobs (NOW HIRING)

Prepare regulatory documents for new study submissions to IRB and sponsor * Maintain regulatory ... Our comprehensive benefits package for full-time employees includes medical, dental, and vision ...

New

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

... such as IRB/FDA processes, research administration, and sponsor collaboration. Location: Good Samaritan Hospital 375 Dixmyth Ave, Cincinnati, OH 45220 Schedule: Full time, day shift Incentives ...

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

... such as IRB/FDA processes, research administration, and sponsor collaboration. Location: Good Samaritan Hospital 375 Dixmyth Ave, Cincinnati, OH 45220 Schedule: Full time, day shift Incentives ...

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

... such as IRB/FDA processes, research administration, and sponsor collaboration. Location: Good Samaritan Hospital 375 Dixmyth Ave, Cincinnati, OH 45220 Schedule: Full time, day shift Incentives ...

Good Samaritan Hospital at 375 Dixmyth Avenue Work Schedule: * Full-Time (80 hours bi-weekly) * Day ... Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA ...

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

... such as IRB/FDA processes, research administration, and sponsor collaboration. Location: Good Samaritan Hospital 375 Dixmyth Ave, Cincinnati, OH 45220 Schedule: Full time, day shift Incentives ...

Good Samaritan Hospital at 375 Dixmyth Avenue Work Schedule: * Full-Time (80 hours bi-weekly) * Day ... Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA ...

Showing results 21-40

Full Time Irb information

See salary details

$62K

$330.1K

$400K

How much do full time irb jobs pay per year?

As of Aug 12, 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 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.

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 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.
More about Full Time Irb jobs
What cities are hiring for Full Time Irb jobs? Cities with the most Full Time Irb job openings:
What are the most commonly searched types of Irb jobs? The most popular types of Irb jobs are:
What states have the most Full Time Irb jobs? States with the most job openings for Full Time Irb jobs include:
Infographic showing various Full Time Irb job openings in the United States as of August 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $330,066 per year, or $158.7 per hour.

Research Compliance Specialist II

Huron Consulting Group

Chicago, IL • Remote

$72K - $88K/yr

Full-time

Medical, Dental, Vision

Posted 15 days ago


Huron Consulting Group rating

7.2

Company rating: 7.2 out of 10

Based on 7 frontline employees who took The Breakroom Quiz

54th of 72 rated business consultants


Job description

Huron helps its clients drive growth, enhance performance and sustain leadership in the markets they serve. We collaborate with education organizations to develop strategies and implement solutions that enable the transformative change our clients need to own their future. Together, we empower clients to drive innovation, create sustainable funding streams and deliver better student outcomes.
Today, leaders of higher education institutions and academic medical centers are spending too much time reacting to market forces, rather than focusing on the essential priorities that help students, faculty and staff thrive. The most productive path forward requires an intentional approach and innovative thinking, whereby stakeholders across the entire institution rally around a shared vision and embrace the hard work of effecting change.
You'll help our clients to achieve organizational effectiveness, improve student outcomes, implement new technologies and align resources and investments to ensure long-term sustainability.
Join our team as the expert you are now and create your future.

Research Office, developed by Huron Consulting Group, is a comprehensive solution designed to streamline research administration and compliance for institutions engaged in sponsored research. We proudly partner with academic medical centers, children's hospitals, health systems, research universities, and sponsors. Our work is powered by proprietary technology and a deep bench of subject matter experts, enabling us to drive efficiency and elevate outcomes across the research enterprise.
Joining the Huron team means you'll help our clients evolve and adapt to the rapidly changing research environment and drive optimization in the existing business operations.
Are you ready to make an impact on the research compliance industry? As a member of Huron's Research Office team, you will apply your knowledge of federal research compliance regulations to provide support for universities, academic medical centers and hospitals across the country.
You will use your time management skills to work on multiple clients concurrently and apply your expertise and work ethic to process and review Institutional Review Board (IRB) submissions and conflict of interest (COI) disclosures. You will apply guidelines and client specific requirements to coordinate and process the reviews. Bring your expertise and be part of the Huron Higher Education team with opportunities to collaborate, learn and grow while impacting some of the most prestigious higher education institutions. This is a dynamic environment where new challenges present themselves daily and no two days are the same.

Essential Duties:

  • Reviews and triages incoming items including IRB submissions (requests for determination/approval, new information, and questions, concerns, and complaints of investigators, research staff, IRB members, subjects, and other individuals) and COI disclosures.
  • Conducts pre-review of IRB submissions to determine federal agency oversight, evaluate for missing materials, and identifies special regulatory issues that will need to be handled by the IRB.
  • Conducts certain non-committee IRB reviews (e.g. not human research and exempt determinations).
  • Supports COI disclosure process, including initiating disclosure cycles and escalating non-compliance with disclosure timeliness.
  • Reviews and evaluates COI disclosures against research portfolios and institutional responsibilities and identifies disclosures that need to be reviewed by a COI Committee or other leader as required by institutional policy.
  • Drafts COI management plans.


Required Qualifications:

  • U.S. work authorization required.
  • Huron requires a bachelor's degree for this position or equivalent work experience.
  • A minimum of 2 years of combined IRB and COI experience.
  • Proficiency in Microsoft Word, Adobe Acrobat other applications of the Microsoft Office suite. Strong proficiency in Microsoft Excel.
  • Proficiency in working with electronic IRB and COI submission/review systems.
  • Knowledge of federal regulations governing the ethical conduct of research and the protection of human subjects.
  • Knowledge of conflict of interest federal regulations.
  • Effective time management to meet deadlines.
  • Ability to multi-task, supporting multiple internal initiatives at one time.
  • Excellent oral and written communication skills, ability to learn quickly and attention to detail
  • This is a full time US-REMOTE role. This salaried position may require working additional hours at times, depending on business needs.


Preferred Qualifications:

  • Certification as an IRB Professional (CIP)
  • Prior experience using the Huron HRPP Toolkit
  • Prior experience using HRS IRB and/or COI software

The estimated base salary range for this job is $72,000 - $88,000. The range represents a good faith estimate of the range that Huron reasonably expects to pay for this job at the time of the job posting. The actual salary paid to an individual will vary based on multiple factors, including but not limited to specific skills or certifications, years of experience, market changes, and required travel. This job is also eligible to participate in Huron's annual incentive compensation program, which reflects Huron's pay for performance philosophy. Inclusive of annual incentive compensation opportunity, the total estimated compensation range for this job is $77,760 - $98,60. The job is also eligible to participate in Huron's benefit plans which include medical, dental and vision coverage and other wellness programs. The salary range information provided is in accordance with applicable state and local laws regarding salary transparency that are currently in effect and may be implemented in the future.

Position LevelSenior AnalystCountryUnited States of America

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About Huron Consulting Group

Sourced by ZipRecruiter

Huron Consulting Group, based in Chicago, IL, US, is a leading global management consulting firm specialized in providing performance improvement and reformation skills to different types of organizations. The company operates in the management consulting industry, which includes strategy, operations, technology, and analytics. Founded in 2002, Huron Consulting Group aids entities to tackle complex business challenges, enhance their ability to drive change, encourage their efficiency, and stimulate innovation. The company's overriding mission is to assist clients in becoming more successful.

Industry

Business management consulting

Company size

1,001 - 5,000 Employees

Headquarters location

Chicago, IL, US

Year founded

2002