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Irb Analyst Jobs in Minnesota (NOW HIRING)

AP Research Tutor

Edina, MN · Remote

$18 - $40/hr

... analysis, academic writing conventions, and oral presentation techniques. Ability to explain ... IRB ethical requirements, and integrating multiple sources into a cohesive literature review.

AP Research Tutor

Saint Paul, MN · Remote

$18 - $40/hr

... analysis, academic writing conventions, and oral presentation techniques. Ability to explain ... IRB ethical requirements, and integrating multiple sources into a cohesive literature review.

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Irb Analyst information

See Minnesota salary details

$30.4K

$71.8K

$127.3K

How much do irb analyst jobs pay per year?

As of Aug 17, 2026, the average yearly pay for irb analyst in Minnesota is $71,753.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,400.00 and $85,200.00 per year, depending on experience, location, and employer.

What is an IRB analyst?

An IRB (Institutional Review Board) Analyst is responsible for reviewing research proposals to ensure they comply with ethical guidelines and regulatory requirements for human subjects' protection. They assess study protocols, verify informed consent procedures, and ensure adherence to federal and institutional policies. IRB Analysts collaborate with researchers to address compliance issues and provide guidance on ethical research practices. Their role is critical in safeguarding participants' rights and welfare while facilitating ethical research.

What are the key skills and qualifications needed to thrive as an IRB analyst?

To thrive as an IRB Analyst, you need a strong background in research ethics, regulatory compliance, and an understanding of human subjects research, often supported by a relevant bachelor's or master's degree. Familiarity with electronic protocol management systems, federal regulations (such as the Common Rule), and certifications like CIP (Certified IRB Professional) are highly valued. Strong attention to detail, analytical thinking, and effective communication skills set outstanding IRB Analysts apart. These qualities are crucial to ensure thorough, ethical review of research protocols and strict adherence to regulatory standards, protecting the rights and welfare of research participants.

What are some common challenges faced by IRB analysts in their daily work?

IRB Analysts frequently navigate complex regulatory requirements while reviewing a diverse range of research protocols, which can present challenges in interpreting guidelines and ensuring full compliance. They must balance efficiency with thoroughness, often working under tight deadlines to support both researchers and institutional standards. Staying current with evolving ethical standards and federal regulations is essential, as is effectively communicating decisions to investigators who may have varying levels of experience. Despite these challenges, the IRB Analyst role is rewarding for those who value ethical oversight and enjoy collaborative, detail-oriented work.

What do you need to be an IRB analyst?

To become an IRB analyst, candidates typically need a bachelor's degree in a related field such as healthcare, research, or ethics, along with experience in research compliance or regulatory environments. Knowledge of federal regulations like the Common Rule and Good Clinical Practice (GCP) is essential, and certifications such as the Certified IRB Professional (CIP) can enhance qualifications. Strong attention to detail, analytical skills, and the ability to review research protocols are also important for the role.

What does an IRB analyst do?

An IRB analyst reviews research protocols to ensure they comply with ethical standards and regulatory requirements set by Institutional Review Boards. They evaluate study procedures, consent forms, and risk assessments, often using specialized software, to protect research participants and maintain compliance. IRB analysts typically have a background in research ethics, healthcare, or related fields and work closely with researchers and regulatory bodies.

What are the most commonly searched types of Irb Analyst jobs in Minnesota?

The most popular types of Irb Analyst jobs in Minnesota are:

What are popular job titles related to Irb Analyst jobs in Minnesota?

For Irb Analyst jobs in Minnesota, the most frequently searched job titles are:

What cities in Minnesota are hiring for Irb Analyst jobs?

Cities in Minnesota with the most Irb Analyst job openings:

Infographic showing various Irb Analyst job openings in Minnesota as of August 2026, with employment types broken down into 80% Full Time, 13% Part Time, and 7% Contract. Highlights an 66% In-person, 7% Hybrid, and 27% Remote job distribution, with an average salary of $71,753 per year, or $34.5 per hour.

PSG Tech and Clinical Research Coordinator

University of Minnesota

Minneapolis, MN

$25.25 - $33.75/hr

Full-time

Medical, Dental, Life, Retirement

Re-posted 17 days ago


Job description

About the Job
 

Position Summary: This position will serve as a PSG sleep technologist and Clinical Research Coordinator for a Sleep Neurologist who studies the relationship between sleep and Alzheimer's disease pathology. This position requires some experience or education as a Sleep technologist and will provide research participant care and education about sleep studies within the framework of a research trial. This role requires setting up specialized monitoring equipment for home based sleep studies and analyzing sleep stages and respiratory events. Main duties include setting up home based sleep studies, education of participants in sleep equipment and troubleshooting equipment issues with participants, analyzing data, and ensuring all data handling complies with privacy rules. The role will also support the investigator as a Clinical Research professional coordinating clinical research trials in treatment of sleep disorders, under PI supervision. 

The person who takes this position may be responsible for multiple research studies simultaneously, coordinating with the PI, IRB, sponsoring agency, community and the study participants. The role will be responsible for coordinating and recording all phases of study protocol as required by GCP and sponsoring agencies to ensure compliance. This role will be in person 2-3 days per week at the University of MN, Twin Cities campus and at clinical sites within the Twin City Metro area. Visa sponsorship and/or relocation assistance not available for this position. 

Work Schedule: Hybrid (predominately in-person), 7:30am - 4pm, M-F

Duties/Responsibilities: 
40% Sleep technologist: 

  • Follow protocol guidelines when collecting sleep data using polysomnography, home sleep testing, single-channel EEG devices and actigraphy.
  • Score sleep research studies.
  • Generates reports and enters data into electronic databases per protocol.
  • Ensures secure data storage of all study materials.


40% Clinical Research Coordinator:

  • Coordinates all aspects of investigator-initiated research and clinical trials with the principal investigator and senior clinical research coordinator. 
  • Identify, recruit, screen, obtain informed consent, educate, monitor, and follow-up with subjects.
  • Under PI supervision, contribute in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews. 
  • Work directly with study participants educating about diagnostic procedures and study procedures and plans, explaining purpose of study and obtains consent.
  • Completed study documentation following ALCOA and GCP standards.
  • Addresses participant concerns, study issues, trouble shoots study issues and ensures PI is properly informed. Communicate with PI, Sponsor, IRB and other regulatory groups and participants as needed to ensure safety, adherence to protocol, AEs, SAES and understanding of studies.
  • Duties must be completed in a timely manner and must comply with protocol guidelines, Good Clinical Practices (GCP), all applicable University guidelines, Standard operation procedures (SOPs), laws, and requirements of regulatory agencies. 


7.5% Scheduling and Communication:

  • Follow protocol to schedule study participants and timely completion of all protocol requirements (assessment, lab testing, procedures and treatments). 
  • Addresses participant concerns, trouble shoots study related issues and ensures PI is properly informed. 
  • Communicate with PI, Sponsor, IRB and other regulatory groups and participants as needed to ensure safety, adherence to protocol, AEs, SAES and understanding of studies.

7.5% Regulatory and Compliance:

  • Comply with protocol guidelines, Good Clinical Practices (GCP), all applicable University guidelines, Standard operation procedures (SOPs), laws, and requirements of regulatory agencies. 
  • Coordinate site visits with industry sponsors; coordinate communications with funding or sponsoring agencies.
  • Under supervision by lead coordinator, coordinate IRB submissions, continuing annual reviews and Serious Adverse Event reporting (SAE); assist with protocol correction action plans as appropriate.


5% Other duties as needed:

  • Performs other duties in addition to the work described above
     
Qualifications
 

All required qualifications must be included in the application materials

Required Qualifications:

  • BA\BS in a psychology, neuroscience, biology or health related field, or a combination of education and experience to equal at least 4 years of relevant experience. 
  • Experience scoring polysomnographic studies.
  • Relevant training or working experience as a sleep technologist. 
  • Prior work experience,  or interest in clinical research support.
  • Effective analytical and problem solving skills.
  • Organized with excellent attention to detail.
  • Excellent verbal and written communication skills.
  • Must demonstrate independence and interpersonal skills.
  • Ability to prioritize tasks within a diverse working environment. 
  • Must comply with applicable laws, regulations, guidelines and standards regarding patient safety and infection control.
  • Willing to work on site (Twin Cities) at least 2-3 days per week.

Preferred Qualifications: 

  • 1 year of experience working as a sleep technologist.
  • 1 year of experience in clinical research.
About the Department
 

To learn more about the Department of Neurology, please visit https://med.umn.edu/neurology. 

Pay and Benefits
 

Pay Range: $31.73/hr - $38.47/hr; depending on education/qualifications/experience

Time Appointment: 100% Appointment

Position Type: Civil-Service & Non-Faculty Labor Represented Staff

Please visit the Office of Human Resources website for more information regarding benefit eligibility.

The University offers a comprehensive benefits package that includes:

  • Competitive wages, paid holidays, and generous time off
  • Continuous learning opportunities through professional training and degree-seeking programs supported by the Regents Tuition Benefit Program
  • Low-cost medical, dental, and pharmacy plans
  • Healthcare and dependent care flexible spending accounts
  • University HSA contributions
  • Disability and employer-paid life insurance
  • Employee wellbeing program
  • Excellent retirement plans with employer contribution
  • Public Service Loan Forgiveness (PSLF) opportunity
  • Financial counseling services 
  • Employee Assistance Program with eight sessions of counseling at no cost
  • Employee Transit Pass with free or reduced rates in the Twin Cities metro area

While our salary ranges provide a framework, it is important to note that most of the time, the initial pay may not reach the maximum of the range. This approach ensures that compensation reflects the value and unique contributions of each candidate while maintaining equity within our organization. As part of our commitment to fair and equitable compensation, please be aware that the salary offered to incoming candidates will be based on their individual credentials and experience.

How To Apply
 

Applications must be submitted online.  To be considered for this position, please click the Apply button and follow the instructions.  You will be given the opportunity to complete an online application for the position and attach a cover letter and resume.

Additional documents may be attached after application by accessing your "My Job Applications" page and uploading documents in the "My Cover Letters and Attachments" section.

To request an accommodation during the application process, please e-mail employ@umn.edu or call (612) 624-8647.

Diversity
 

The University recognizes and values the importance of diversity and inclusion in enriching the employment experience of its employees and in supporting the academic mission.  The University is committed to attracting and retaining employees with varying identities and backgrounds.

The University of Minnesota provides equal access to and opportunity in its programs, facilities, and employment without regard to race, color, creed, religion, national origin, gender, age, marital status, disability, public assistance status, veteran status, sexual orientation, gender identity, or gender expression.  To learn more about diversity at the U:  http://diversity.umn.edu

Employment Requirements
 

Any offer of employment is contingent upon the successful completion of a background check. Our presumption is that prospective employees are eligible to work here. Criminal convictions do not automatically disqualify finalists from employment.

About University of Minnesota
 

The University of Minnesota, Twin Cities (UMTC)

The University of Minnesota, Twin Cities (UMTC), is among the largest public research universities in the country, offering undergraduate, graduate, and professional students a multitude of opportunities for study and research. Located at the heart of one of the nation's most vibrant, diverse metropolitan communities, students on the campuses in Minneapolis and St. Paul benefit from extensive partnerships with world-renowned health centers, international corporations, government agencies, and arts, nonprofit, and public service organizations.

At the University of Minnesota, we are proud to be recognized by Forbes as a Best Employer for Company Culture (2026), Best Employer for Women (2023, 2025, 2026), and Best Employer by State (2022-2026). In 2026, we also received Culture Excellence & Industry Awards recognition for employee appreciation and work-life flexibility.