Jobs and Careers
UN
Research Data Analysts
University of UtahSalt Lake City, United Statespart_timeVerifiedPosted 29 May 2026
💰 $48,000/yr($42,000/yr – $48,000/yr)
About the role
Details
Open Date
05/29/2026
Requisition Number
PRN17116N
Job Title
Research Data Analysts
Working Title
Quantitative Research Data Analyst
Career Progression Track
P00
Track Level
P3 - Career, P2 - Developing, P1 - Entry Level Pro
FLSA Code
Administrative
Patient Sensitive Job Code?
No
Type
Non Benefited Staff / Student
Temporary?
No
Standard Hours per Week
19
Full Time or Part Time?
Part Time
Shift
Day
Work Schedule Summary
Is this a work study job?
No
VP Area
U of U Health - Academics
Department
00870 - Ophthalmology-Research
Location
Campus
City
Salt Lake City, UT
Type of Recruitment
External Posting
Pay Rate Range
$21.00 - $24.00
Close Date
08/01/2026
Priority Review Date (Note - Posting may close at any time)
Job Summary
We are seeking a highly motivated Quantitative Research Data Analyst to support epidemiological and clinical research studies using diverse healthcare and population-based datasets. The successful candidate will contribute to all phases of quantitative research, including data management, statistical analysis, manuscript preparation, and mentoring trainees in a collaborative academic research environment.
Responsibilities
Essential Functions:
• Lead quantitative research activities under the guidance of the Principal Investigator (PI), including data cleaning, data management, sample size calculations, and statistical analyses for observational studies and clinical trials.
• Conduct epidemiological analyses using advanced statistical methods, including regression modeling and survival analysis techniques.
• Analyze and interpret data from electronic health records (EHR), survey data, administrative healthcare claims, clinical trial datasets, and national survey datasets.
• Prepare statistical results, tables, figures, and written summaries for manuscripts, reports, abstracts, and scientific presentations.
• Contribute to the preparation and submission of grant applications, Institutional Review Board (IRB) protocols, amendments, and related regulatory documentation to support the ethical conduct of research studies.
• Support quantitative data management activities using REDCap, including survey development, data collection, quality assurance, and data export procedures.
• Assist with participant recruitment, study enrollment, and informed consent processes as needed particularly for surveys
• Mentor and supervise student volunteers and trainees interested in quantitative and clinical research.
• Contribute to conference presentations, scientific posters, and peer-reviewed publications.
• Participate in additional research-related activities that align with project needs and individual strengths.
Minimum Qualifications
• Lead quantitative research activities under the guidance of the Principal Investigator (PI), including data cleaning, data management, sample size calculations, and statistical analyses for observational studies and clinical trials.
• Conduct epidemiological analyses using advanced statistical methods, including regression modeling and survival analysis techniques.
• Analyze and interpret data from electronic health records (EHR), survey data, administrative healthcare claims, clinical trial datasets, and national survey datasets.
• Prepare statistical results, tables, figures, and written summaries for manuscripts, reports, abstracts, and scientific presentations.
• Contribute to the preparation and submission of grant applications, Institutional Review Board (IRB) protocols, amendments, and related regulatory documentation to support the ethical conduct of research studies.
• Support quantitative data management activities using REDCap, including survey development, data collection, quality assurance, and data export procedures.
• Assist with participant recruitment, study enrollment, and informed consent processes as needed particularly for surveys
• Mentor and supervise student volunteers and trainees interested in quantitative and clinical research.
• Contribute to conference presentations, scientific posters, and peer-reviewed publications.
• Participate in additional research-related activities that align with project needs and individual strengths.
EQUIVALENCY STATEMENT: 1 year of higher education can be substituted for 1 year of directly related work experience (Example: bachelor’s degree = 4 years of directly related work experience).
Department may hire employee at one of the following job levels:
Research Data Analyst I: Requires a bachelor’s (or equivalency) + 2 years of directly related work experience or a master’s (or equivalency) degree.
Research Data Analyst II: Requires a bachelor’s (or equivalency) + 4 years or a master’s (or equivalency) + 2 years of directly related work experience.
Research Data Analyst III: Requires a bachelor’s (or equivalency) + 6 years or a master’s (or equivalency) + 4 years of directly related work experience.
• Expertise in epidemiological research methods, particularly regression modeling and survival analysis techniques.
• Experience working with large healthcare and research datasets, including EHR data, administrative healthcare claims, clinical trial data, and national survey datasets.
• Proficiency in statistical software such as SAS, Stata, R, SPSS, or similar analytical platforms.
• Experience using REDCap for survey development, data collection, management, and export.
• Strong scientific writing and data visualization skills, including preparation of tables, figures, and manuscript results sections.
• Experience analyzing national survey data and GIS mapping is preferred, but not required.
• Knowledge of vision screening, ophthalmology, optometry, or eye disease research (e.g., amblyopia, glaucoma, diabetic retinopathy) is a plus, but not required.
• Excellent organizational, communication, and collaborative skills with the ability to work independen
• Experience working with large healthcare and research datasets, including EHR data, administrative healthcare claims, clinical trial data, and national survey datasets.
• Proficiency in statistical software such as SAS, Stata, R, SPSS, or similar analytical platforms.
• Experience using REDCap for survey development, data collection, management, and export.
• Strong scientific writing and data visualization skills, including preparation of tables, figures, and manuscript results sections.
• Experience analyzing national survey data and GIS mapping is preferred, but not required.
• Knowledge of vision screening, ophthalmology, optometry, or eye disease research (e.g., amblyopia, glaucoma, diabetic retinopathy) is a plus, but not required.
• Excellent organizational, communication, and collaborative skills with the ability to work independen
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