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Study Coordinator

Regents of the University of Minnesota

Minneapolis, MN · HybridFull-time$55–67K/yrSeen 1 day agoSeen in employer's feed 1 day ago

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At a glance

Compensation
$55–67K/yr
Location
Minneapolis, MNHybrid
Schedule
Full-time
Work Authorization
Not specified

Olive focuses on jobs in the United States, including remote roles you can work from there.

Job overview

The Center for Pediatric Obesity Medicine seeks a full-time Study Coordinator to support a decentralized trial with adolescent participants. The coordinator manages study activities from recruitment and screening through virtual visits, data collection, safety monitoring, and medication coordination. The position is in person initially and will transition to hybrid. Once recruitment begins, evening work until 8 p.m. is required at least three days per week, based on study needs.

Skills & qualifications

RequiredNice to have

Skills

Telehealth Platforms, requiredComputerized Data Management, requiredOrganizational Skills, requiredPlanning, requiredProblem-Solving, requiredIndependent Work, requiredTeamwork, requiredPrioritization, requiredDeadline Management, requiredWritten Communication, requiredVerbal Communication, requiredInterpersonal Skills, requiredAdolescent Research, nice to haveCaregiver Research, nice to haveREDCap, nice to haveOncore Clinical Trials Management System, nice to haveSpanish, nice to haveEnglish, nice to have

Qualifications

BA/BS in Scientific or Health Field or Equivalent Research Education and Experience, required2+ Years Research Experience or 6+ Years Combined Education and Research Experience, requiredProfessional Spanish and English Experience, nice to have

Benefits

Paid Time Off
Tuition Assistance
Medical Insurance
Dental Insurance
401(k) Match

Full job description

Job Duties

Apply for Job

Job ID376562

LocationTwin Cities

Job FamilyResearch

Full/Part TimeFull-Time

Regular/TemporaryRegular

Job Code8352RG

Employee ClassCivil Service

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About the Job

About the Job

The Center for Pediatric Obesity Medicine (CPOM) seeks a full time Study Coordinator to support a high-volume decentralized trial with adolescent participants. CPOM is a multidisciplinary research center dedicated to improving outcomes for youth navigating obesity and its related conditions. This position will be responsible for the day-to-day activities of the study, including screening and enrolling participants, conducting virtual study visits, collecting data, maintaining data integrity and safety monitoring, and working closely with study partners.

This is an in-person position that will transition to hybrid in the future. Once recruitment begins, this position requires working evenings (until 8 pm) at least three days per week, based on study needs.

Responsibilities:

Clinical Research Project Coordination (50%)

Coordinate all aspects of study participation throughout the full life-cycle of the trial, including recruitment and screening, determining eligibility, conducting informed consent (with parents) and assent (with adolescents), scheduling, and conducting virtual participant visits

Lead structured virtual study visits via secure telehealth platforms, maintaining a professional clinical environment in a remote setting

Track participant payment cards and initiate payments after study visits

Facilitate the timely review and reporting of adverse reactions and serious adverse events

Provide basic troubleshooting for study-provided technology

Actively participate in weekly study team meetings to report on enrollment progress, participant challenges, technological troubles, and other related topics

Identify potential gaps or concerns in the workflows and suggest practical changes for improvement to the study's leadership team

Additional study-related activities, as assigned

Data Collection (30%)

Oversee the collection of participant-reported outcome surveys

Administer surveys to and conduct interviews with study participants

Maintain high quality source documentation and participant files

Promptly and accurately enter participant data in databases

Clinical Intervention & Supply Coordination (20%)

Under the supervision of the study physicians, instruct participants on how to administer study medications and proper disposal of used medical pens

Initiate and track study medication orders through the Investigational Drug Services pharmacy

Proactively resolve issues related to medication delivery and participant receipt of study materials

Routinely assess participant medication compliance, utilizing motivational interviewing and education to troubleshoot adherence barriers

Coordinate remote laboratory visits; ensure participants receive transportation vouchers and instructions for blood draws and biometric measurements

Monitor participants for adverse events and changes in health status.

Essential Employees: The successful candidate will be designated as an Essential Employee. Essential Employees are expected to report to campus during a University State of Emergency (reduced operations or campus closure) unless specifically directed by the Department not to report or if directed by civil emergency or medical authorities not to report for health and safety reasons. As an Essential Employee, you must report to campus even if the closure is less than 3 days.

Qualifications

All required qualifications must be documented on application materials

Required Qualifications:

BA/BS in a scientific or health related field and at least 2 years research experience OR a combination of education and experience in research to equal at least 6 years

Expertise in telehealth platforms and demonstrated experience with computerized data management

Detail-oriented with exceptional organizational, planning, and problem-solving skills

Ability to work independently, as a part of a team, and with changing priorities

Demonstrated ability to maintain deadlines and prioritize assignments

Excellent written, verbal, and interpersonal skills, including in a virtual environment

Preferred Qualifications:

Experience working with adolescents and their caregivers in a research or high-volume clinical setting

Experience with REDCap data management and Oncore Clinical Trials Management System

Bilingual Spanish/English speaker with experience speaking both languages in a professional setting

Pay and Benefits

Pay Range: $55,000 - $67,000/year; depending on education/qualifications/experience

Time Appointment: 100% Appointment (Hybrid)

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].

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 of Minnesota Medical School

Committed to innovation and diversity, the Medical School educates physicians, scientists, and health professionals; generates knowledge and treatments; and cares for patients and communities with compassion and respect. We value excellence, inclusiveness, collaboration, and discovery.

The mission of the regional campus located in Duluth is to be a national leader in improving healthcare access and outcomes in rural Minnesota and American Indian/Alaska Native (AI/AN) communities. In partnership with CentraCare, the regional campus in St. Cloud offers a wide range of patient experiences throughout students' education in Greater Minnesota and prepares them to become exceptional clinicians and leaders for rural and immigrant populations.

Founded in 1888, the University of Minnesota Medical School has three campuses. A four-year MD program and the MD/PhD program are located on the Twin Cities campus in addition to MD programs at regional campuses in Duluth and St. Cloud.

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

2 - 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

376562

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$55–67K/yr
  • US median$56–77K/yr180 salary ranges

This range's midpoint, $61K, is 8% below the US median midpoint ($66K) — in the middle half of Clinical Research Coordinator salary 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
Experience
This posting asks for at least 2 years of experience; Clinical Research Coordinator postings that state a minimum ask for 2 years at the median (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.

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