Skip to main content
Regents of the University of Minnesota logo

Rsch Pro 2-Rsch Coord-Cln I/T

Regents of the University of Minnesota

Minneapolis, MN · HybridFull-time$55–65K/yrSeen 1 day agoSeen in employer's feed 1 day ago

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.

Don't just apply. Show up ready.

Olive works from this exact posting.

At a glance

Compensation
$55–65K/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 Research Coordinator supports clinical studies and trials across multiple pediatric specialties, coordinating patient enrollment and study visits, managing data and specimens, and handling regulatory requirements. The role collaborates with investigators, providers, clinical teams, and study staff to maintain compliant, high-quality research and support study start-up, quality improvement, and research dissemination.

Skills & qualifications

RequiredNice to have

Skills

Clinical Research Coordination, requiredInformed Consent, requiredGood Clinical Practices, requiredFederal Clinical Research Regulations, requiredComputerized Data Management, requiredElectronic Medical Records, requiredOrganization, requiredPlanning, requiredProblem-Solving, requiredIndependent Work, requiredTeamwork, requiredPrioritization, requiredDeadline Management, requiredWritten Communication, requiredVerbal Communication, requiredInterpersonal Skills, requiredData Collection, nice to haveData Entry, nice to haveData Quality, nice to haveSpecimen Management, nice to haveHuman Sample Processing, nice to haveRegulatory Management, nice to haveIRB Submissions, nice to haveRegulatory Binder Maintenance, nice to haveStanding, requiredWalking, requiredReaching, requiredLifting, requiredCarrying, required

Qualifications

BA/BS in Scientific or Health Field or Equivalent Research Education and Experience, required2 Years Research Experience, required

Benefits

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

Full job description

Job Duties

Apply for Job

Job ID376297

LocationTwin Cities

Job FamilyResearch

Full/Part TimeFull-Time

Regular/TemporaryRegular

Job Code8352RC

Employee ClassCivil Service

Add to Favorite Jobs

Email this Job

About the Job

The primary purpose of this position is to support clinical studies, including clinical trials, within multiple pediatric specialties according to regulatory requirements, institutional guidelines, and sponsor expectations. Duties include initiating new studies, coordinating the enrollment of eligible patients, conducting study visits, extracting and reporting quality patient data and tissue samples, performing regulatory management, and responding to data queries.

Responsibilities:

Clinical Research Project Coordination (70%)

Coordinate patient participation in clinical research, including screening and recruiting patients and families, ensuring study eligibility and enrollment, scheduling and conducting research visits

Data collection and submission for multiple projects, including engaging with providers and investigators to ensure adequate source documentation is available; accurate interpretation and recording of data; maintenance of subject research charts

Specimen management for multiple projects including facilitating the collection of research

specimens during routine clinical procedures, ensuring high quality processing of research specimens, and coordinating timely and compliant shipment of research specimens to research laboratories

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

Contribute to the production of research publications or presentations of research data

Additional study-related activities, as assigned.

Regulatory (20%)

Prepare regulatory submissions in collaboration with the PI including continuing reviews, protocol amendments, and consent form modifications

Support the maintenance of regulatory binders and required documentation for each clinical research study to ensure compliance and to be audit-ready at any given time

Prepare for and participate in site initiation visits, monitoring visits, program audits, etc.

Report Unanticipated Problems according to University policy

Administration and Education (10%)

Support new project development and study start-up activities

Support quality improvement initiatives

Serve as mentor and share knowledge with other study coordinators and study team members

Communicate with clinical teams to foster an environment of quality research participation within the context of exceptional clinical care

Attends local and national study meetings as appropriate

Qualifications

All required qualifications must be documented on application materials

Required Qualifications:

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

Experience as a research coordinator in clinical research, including obtaining informed consent

Working knowledge of Good Clinical Practices (GCPs), and federal regulations related to clinical research

Experience with computerized data management, preferably in a health-related setting and including experience with electronic medical records

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

During a typical 8 hour shift, a person in this position may be required to stand up to 2.5 hours, walk up to 2.5 hours (including stairs), reach above shoulders, lift up to 10 pounds above the shoulder, and carry packages across campus at waist level.

Preferred Qualifications:

Experience with computerized data management, preferably in a health-related setting and including experience with electronic medical records

Demonstrated data management skills, including data collection, data entry, and ensuring data quality

Specimen management experience including processing human samples and shipping per regulations

Regulatory management experience including IRB submissions and regulatory binder maintenance

Pay and Benefits

Pay Range: $55,000 - $65,000/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

376297

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$55–65K/yr
  • US median$56–77K/yr180 salary ranges

This range's midpoint, $60K, is 9% 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.

Prepare for this role

You've read the whole posting — now see how you match it.