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Clinical Statistical Programmer Jobs in Kansas (NOW HIRING)

micro1 AI

Director of Biostatistics

Topeka, KS · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

Wichita, KS · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

Kansas City, KS · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

Overland Park, KS · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

Olathe, KS · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Parexel

From clinical trials to regulatory, consulting, and market access, every clinical development ... Leverage advanced statistical and epidemiological methodologies to deliver robust and reliable ...

Altasciences

Biostatistician II

Overland Park, KS · On-site

$70K - $90K/yr

Development of tables of summary statistics and graphics for clinical aspects of clinical trials ... Moderate SAS programming proficiency. Altasciences strives to provide a French working environment ...

Altasciences

Biostatistician II

Overland Park, KS · On-site +1

$70K - $90K/yr

Development of tables of summary statistics and graphics for clinical aspects of clinical trials ... Moderate SAS programming proficiency. Altasciences strives to provide a French working environment ...

micro1 AI

Director of Biostatistics

Overland Park, KS · Remote

$60 - $100/hr

MS or PhD in biostatistics, statistics, or epidemiology. * 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts. * Demonstrated command of clinical ...

micro1 AI

Director of Biostatistics

Kansas City, KS · Remote

$60 - $100/hr

MS or PhD in biostatistics, statistics, or epidemiology. * 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts. * Demonstrated command of clinical ...

micro1 AI

Director of Biostatistics

Wichita, KS · Remote

$60 - $100/hr

MS or PhD in biostatistics, statistics, or epidemiology. * 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts. * Demonstrated command of clinical ...

micro1 AI

Director of Biostatistics

Topeka, KS · Remote

$60 - $100/hr

MS or PhD in biostatistics, statistics, or epidemiology. * 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts. * Demonstrated command of clinical ...

micro1 AI

Director of Biostatistics

Olathe, KS · Remote

$60 - $100/hr

MS or PhD in biostatistics, statistics, or epidemiology. * 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts. * Demonstrated command of clinical ...

Nordic

The data scientist collaborates with business partners (clinicians / supply chain / HR across ... Doctorate, Data Science, Computer Science, Engineering, or Statistics (preferred) * Experience ...

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All JobsClinical Statistical Programmer JobsClinical Statistical Programmer Jobs in Kansas

Clinical Statistical Programmer information

See Kansas salary details

$14

$48

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How much do clinical statistical programmer jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical statistical programmer in Kansas is $48.32, according to ZipRecruiter salary data. Most workers in this role earn between $30.67 and $72.69 per hour, depending on experience, location, and employer.

What does a clinical statistical programmer do?

A Clinical Statistical Programmer is responsible for managing and analyzing clinical trial data using statistical software, such as SAS or R. Their primary tasks include creating datasets, programming statistical analyses, and generating tables, listings, and figures for clinical study reports. They work closely with biostatisticians and clinical research teams to ensure data accuracy and regulatory compliance. Their work is essential for supporting submissions to regulatory agencies and for making data-driven decisions in clinical research.

What does a clinical statistical programmer do?

The job duties of a clinical statistical programmer involve collecting data, performing statistical analysis, and analyzing data sets according to the needs of their employer or client. Your responsibilities in this career may involve using SAS programming to create and analyze data sets during clinical trials or other clinical experiments and studies. You may also be involved in performing data integration for reports following clinical research or statistical analysis for quality control (QC).

What are the key skills and qualifications needed to thrive as a clinical statistical programmer, and why are they important?

To thrive as a Clinical Statistical Programmer, you need strong proficiency in statistical programming languages (such as SAS or R), a background in statistics or life sciences, and familiarity with clinical trial processes. Experience with CDISC standards (SDTM, ADaM), regulatory submission requirements, and version control systems is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring data quality. These skills ensure the accurate analysis and reporting of clinical data, which is critical for regulatory compliance and successful clinical trial outcomes.

What are some common challenges faced by clinical statistical programmers when working with clinical trial data?

Clinical Statistical Programmers often encounter challenges such as handling large and complex datasets, ensuring data integrity, and adhering to strict regulatory guidelines (like CDISC standards). Collaborating closely with biostatisticians, data managers, and clinical teams is essential to resolve data discrepancies and meet tight project deadlines. Staying updated on evolving regulatory requirements and software tools is also vital to maintain high-quality deliverables in a fast-paced environment.
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Clinical Statistical Programmer jobs near you
Infographic showing various Clinical Statistical Programmer job openings in Kansas as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $100,507 per year, or $48.3 per hour.

Statistician I - Biostatistics & Data Science

University of Kansas Medical Center

Kansas City, KS • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago

Job description

Department:
SOM Department of Biostatistics
Master Level StatPosition Title:
Statistician I - Biostatistics & Data ScienceJob Family Group:
Professional StaffJob Description Summary:
Under the guidance of a faculty Biostatistician/Data Scientist, the Statistician I will carry out data preparation responsibilities related to basic, clinical and/or population health research; perform introductory to intermediate-level statistical analysis and programming associated with research projects; and assist with the preparation of written reports, manuscripts, and grant applications with investigators.Job Description:
Job Duties
  • Compiles, analyzes, and reports statistical data for various projects including, but not limited to, manual and computer-aided data abstraction and evaluation, clinical trial design, computerized imaging, bioinformatics, and computational genomics.
  • Assists with database preparation and various statistical aspects of investigator-initiated trials, research projects, and grants.
  • Performs basic statistical analysis using appropriate methods, and carries out advanced statistical analyses under the supervision and guidance of Biostatistics faculty member. Assists with the creation, verification, testing, modifying, and certification of the eCRF creation process related to clinical research to ensure quality data collection.
  • Applies basic statistical methods, simulation models, and skilled statistical programming, as needed.
  • Assesses relevant literature as well as existing data, evaluates the quality of data used in reports, and assists with preparation and distribution of data for committee and scientific meetings.
  • Attends project meetings with collaborators and Biostatistics & Data Science faculty members and makes presentations as needed.
  • Prepares written reports, manuscripts, and grant applications for investigators under the supervision of Biostatistics & Data Science faculty.
  • Provide Core Support (ex. Hematological Malignancies and Cellular Therapeutics (HMCT) Core) by assisting investigators with data management, data harmonization, cohort development, statistical programming, and generation of analytic datasets for clinical, translational, and population health research projects.
  • Participates in Heartland Data Coordinating and Operations Center (DCOC) data operations, including data cleaning, quality control (QC), data validation, discrepancy resolution, and preparation of study datasets to ensure data integrity, completeness, and compliance with study protocols and regulatory requirements.
  • Assists with the development and implementation of standard operating procedures (SOPs), data quality metrics, automated QC reports, and monitoring dashboards to support multi-site research studies and centralized data coordinating activities.
  • Collaborates with investigators, data managers, and research staff to identify and resolve data issues, perform routine data audits, and maintain documentation of data management and quality assurance activities.
  • Supports extraction, transformation, integration, and harmonization of data from electronic health records, clinical trial systems, registries, and other research data sources for research and reporting purposes.
  • Contributes to the validation and testing of research databases, electronic case report forms (eCRFs), and data collection workflows to ensure high-quality and reliable data capture across studies.

Required Qualifications
Work Experience:
  • Five (5) years of relevant experience. Relevant education may substitute for experience on a year for year basis.
  • One (1) year of experience with mainframe and/or PC databases, document processing, and statistical software such as SAS, R, Stata, or SPSS.

Preferred Qualifications
Education: Master's Degree in Biostatistics, Statistics, Bioinformatics, Mathematics or related field, or undergraduate degree in similar field of study with at least 5 years of relevant experience.
Work Experience:
  • Three (3) years of experience with mainframe and/or PC databases, document processing, and statistical software.
  • Two (2) years of experience in statistical consulting, data analysis and design related to basic, clinical and/or population health.

Skills
  • Communication skills
  • Organizational skills

Required Documents
  • Resume/CV
  • Cover Letter

Comprehensive Benefits Package:
Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html
Employee Type:
RegularTime Type:
Full timeRate Type:
Salary
Compensation Statement:
The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above.
Pay Range:
$80,600.00 - $120,900.00
Minimum
$80,600.00
Midpoint
$100,800.00
Maximum
$120,900.00

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