
PSG Tech and Clinical Research Coordinator
Regents of the University of Minnesota
Minneapolis, MN · HybridFull-time$31.73–38.47/hrSeen todaySeen in employer's feed today
See where you stand before you apply. No sign-up to start.
You apply on the posting's application page, with no Olive account needed.
Watch jobs like this. New roles like this one near Minneapolis, MN, by email.
Don't just apply. Show up ready.
Olive works from this exact posting.
At a glance
Olive focuses on jobs in the United States, including remote roles you can work from there.
Job overview
This position combines sleep technologist work with clinical research coordination for studies examining sleep disorders and Alzheimer’s disease pathology. The coordinator collects and scores sleep data, supports participants through home-based sleep studies, and coordinates research trials under principal investigator supervision. The role involves protocol and regulatory compliance, participant communication, and coordination with investigators, sponsors, IRB, and clinical sites. Work is hybrid, with in-person work 2–3 days per week at the Twin Cities campus and clinical sites.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Job Duties
Apply for Job
Job ID375395
LocationTwin Cities
Job FamilyResearch
Full/Part TimeFull-Time
Regular/TemporaryRegular
Job Code8351CR
Employee ClassCivil Service
Add to Favorite Jobs
Email this Job
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 [email protected] or call (612) 624-8647.
Diversity
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.
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.
Minimum Education Required
Bachelor Degree
Minimum Experience Required
4 - 20 years
Shift
First (Day)
Number of Openings
1
Public Transportation Accessible
Yes
Veterans Encouraged to Apply
No
Physical Required
Yes
Drug Test Required
Yes
Compensation
$11.41 / Hourly
Postal Code
55455
Job Type
Full Time
Place of Work
On-site
Requisition ID
375395
Job Benefits
Not specified
How this job compares
Set against the 591 open Clinical Research Coordinator jobs on Olive Jobs, counted November 15, 2026.
- Pay
- This posting$31.73–38.47/hr
- US median$25–38/hr193 hourly ranges
This range's midpoint, $35.10/hr, is 17% above the US median midpoint ($30/hr) — in the middle half of Clinical Research Coordinator hourly ranges across the US.
- Openings
- Olive Jobs lists 19 open Clinical Research Coordinator jobs in Minnesota and 591 across the US. 2% of them nationwide are listed as remote or flexible.
- Hiring the most across the US
- Mount Sinai Health System43 open
- Actalent41 open
- University of Miami37 open
- Experience
- This posting asks for at least 4 years of experience — more than three in four Clinical Research Coordinator postings that state a minimum ask for (median 2 years, across 416 postings).
- Education
- 175 of the 591 open Clinical Research Coordinator jobs (30%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 15, 2026. Figures based on too few postings are left out.
Prepare for this role
You've read the whole posting — now see how you match it.


