
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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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
Skills
Qualifications
Benefits
Full job description
Job Duties
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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
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Identifies and reports protocol deviations within the required timeline in accordance with institutional requirements
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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
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Troubleshoots problems in the development and implementation of protocol procedures
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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
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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%)
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Mentors and trains new staff, providing task level guidance to CRCs I and II
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Serves as subject matter experts in key CTO processes
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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
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Ability to work independently, as part of a team, and with changing priorities
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Computer proficiency in a PC environment including Microsoft Office products
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Ability to sit for extended periods of time
PREFERRED QUALIFICATIONS
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Clinical Research Coordinator certification or equivalent
-
Experience with disease-specific research or clinical care
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Experience with patient contact / care
-
Experience abstracting clinical data and familiarity with medical terminology
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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
- Actalent45 open
- Mount Sinai Health System41 open
- Iterative Health37 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 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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