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Clinical Research Coord III

Regents of the University of Minnesota

Minneapolis, MNFull-time$65–77K/yrSeen todaySeen in employer's feed today

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At a glance

Compensation
$65–77K/yr
Location
Minneapolis, MN
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 Clinical Research Coordinator III manages clinical research data collection, study documentation, protocol-required procedures, and collaboration with principal investigators and study teams. The role coordinates trial activities, maintains accurate records and electronic data capture, and mentors newer staff. It requires following Good Clinical Practice and applicable institutional and regulatory guidelines for patient safety and data integrity. Visa sponsorship is not available.

Skills & qualifications

RequiredNice to have

Skills

Attention to Detail, requiredOrganizational Skills, requiredIndependent Work, requiredTeamwork, requiredAdaptability, requiredMicrosoft Office, requiredClinical Research Coordination, nice to haveDisease-Specific Research, nice to havePatient Care, nice to haveClinical Data Abstraction, nice to haveMedical Terminology, nice to haveEpic, nice to haveOnCore, nice to haveOncology, nice to have

Qualifications

BA/BS+4 Yrs, Advanced Degree+2 Yrs, or 8 Yrs Relevant Experience, requiredClinical Research Coordinator Certification or Equivalent, nice to have4 Years Experience, required2 Years Experience, required8 Years Relevant Experience, required

Benefits

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

Full job description

Job Duties

Apply for Job

Job ID374684

LocationTwin Cities

Job FamilyResearch

Full/Part TimeFull-Time

Regular/TemporaryRegular

Job Code8353RC

Employee ClassCivil Service

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About the Job

The Clinical Research Coordinator III is responsible for providing technical expertise and overall management of clinical research data collection, study documentation, protocol-required

procedure execution, and collaboration with PI and study team to ensure consistent and accurate implementation of the protocol. The incumbent will be expected to follow Good Clinical

Practice (GCP) and all organization policies and procedures for patient safety and data integrity, including but not limited to the Institutional Review Board (IRB), Food & Drug Administration (FDA), Code of Federal Regulations (CFR), and International Conference on Harmonization (ICH) guidelines. This position is not eligible for visa sponsorship

SPECIFIC RESPONSIBILITIES

Trial Management / Study Coordination (60%)

  • Interprets protocols and creates source documents needed for clinical research study

  • Identifies and reports protocol deviations within the required timeline in accordance with institutional requirements

  • Ensures protocol adherence by communicating and ensuring study parameters are

executed according to protocol

  • Oversees visits with outside sponsors, including site initiation visits, interim monitoring

visits and closeout visits

  • Collaborates with PI and study team to enroll study participants, execute study-required

procedures, and maintain accurate source documentation

  • Maintains a processing and tracking system for protocol-required biospecimens, data,

and procedures

  • Works as a member of the study team with positive and timely written and verbal

communication, including sharing information up, down, and laterally

  • Troubleshoots problems in the development and implementation of protocol procedures

  • Coordinates with Investigational Drug Services (IDS), BioNet, clinical staff, and other

bodies across campus to deliver drug, collect biospecimens, and execute the study visits

according to protocol

Data Management (25%)

  • Serves as primary contact for the collection and completion of required study

documentation

  • Develops and maintains study documentation to ensure audit-proof compliance

  • Abstracts data from medical record to ensure accurate and complete source

documentation

  • Manages electronic data capture systems, including but not limited to building the case

report forms, responding to queries, and meeting data lock deadlines

  • Demonstrates proficiency with Common Terminology Criteria for Adverse Events

(CTCAE), medical terminology, critical lab values, and other disease-specific diagnostic

criteria

Lead Activities (15%)

  • Mentors and trains new staff, providing task level guidance to CRCs I and II

  • Serves as subject matter experts in key CTO processes

  • Manages additional workload during staff changes

Qualifications

All required qualifications must be documented on application materials.

REQUIRED QUALIFICATIONS

  • BA/BS with at least 4 years of experiences or an advanced degree and 2 years of

experience or 8 years of relevant education & healthcare or research experience

  • Excellent attention to detail and organizational skills

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

  • Computer proficiency in a PC environment including Microsoft Office products

  • Ability to sit for extended periods of time

PREFERRED QUALIFICATIONS

  • Clinical Research Coordinator certification or equivalent

  • Experience with disease-specific research or clinical care

  • Experience with patient contact / care

  • Experience abstracting clinical data and familiarity with medical terminology

  • Experience with Epic, Oncore, or equivalent medical record / Clinical Trial Management

Systems

  • Oncology experience in a clinical or research setting

About the Department

The Masonic Cancer Center (MCC) is an NCI-designated Comprehensive Cancer Center dedicated to cancer research, education, and patient care for the citizens of Minnesota and the surrounding region. Since the time of the first award in 1997, there has been consistent growth of the membership and research base, enabling our center to further advance our knowledge and enhance care for our catchment area. We are driven to be the choice academic healthcare environment for patients, clinicians, scientists and students who seek exceptional, compassionate, precision cancer therapy; innovative clinical trials and prevention programs; cutting-edge research opportunities; and outstanding advanced education.

Pay and Benefits

Pay Range: $65,000 - $77,000 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), 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

374684

Job Benefits

Not specified

How this job compares

Set against the 622 open Clinical Research Coordinator jobs on Olive Jobs, counted November 13, 2026.

Pay
  • This posting$65–77K/yr
  • US median$56–76K/yr170 salary ranges

This range's midpoint, $71K, is 7% above the US median midpoint ($66K) — in the middle half of Clinical Research Coordinator salary ranges across the US.

Openings
Olive Jobs lists 11 open Clinical Research Coordinator jobs in Minnesota and 622 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 4 years of experience — more than three in four Clinical Research Coordinator postings that state a minimum ask for (median 2 years, across 420 postings).
Education
183 of the 622 open Clinical Research Coordinator jobs (29%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 13, 2026. Figures based on too few postings are left out.

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