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Clinical Statistical Programmer Jobs in Kansas (NOW HIRING)

Working closely with members of Data Management, Statistics, Information Technology (IT), and Quality Control (QC) Departments, the Senior Clinical Database Programmer is responsible for the design ...

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

... algorithms/programming * Able to read and understand most SDTM & ADaM domains and mapping ... In-depth knowledge of statistical methodologies and how to apply them in a clinical research ...

Support statistical activities for clinical trials and data analyses, including study design ... programming practices, and regulatory guidelines. * Other duties as assigned. Necessary Skills and ...

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

... clinical trials. • Develop Inferential Statistics. • Potentially support some Statistical ... programming proficiency. Altasciences strives to provide a French working environment for its ...

Lab Supervisor

Lenexa, KS · On-site

$72K/yr

Completes special projects as requested - surveys, statistical reports, studies, research, etc ... Required to use (a) personal protective equipment, (b) engineering controls and/or (c) work ...

Lab Supervisor

Lenexa, KS · On-site

$72K/yr

Completes special projects as requested - surveys, statistical reports, studies, research, etc ... Required to use (a) personal protective equipment, (b) engineering controls and/or (c) work ...

Clinical Statistical Programmer information

See Kansas salary details

$14

$48

$80

How much do clinical statistical programmer jobs pay per hour?

As of Jul 16, 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 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.

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 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 popular job titles related to Clinical Statistical Programmer jobs in Kansas? For Clinical Statistical Programmer jobs in Kansas, the most frequently searched job titles are:
What job categories do people searching Clinical Statistical Programmer jobs in Kansas look for? The top searched job categories for Clinical Statistical Programmer jobs in Kansas are:
What are popular job titles related to Clinical Statistical Programmer jobs in KS? For Clinical Statistical Programmer jobs in KS, the most frequently searched job titles are:
Infographic showing various Clinical Statistical Programmer job openings in Kansas as of July 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% 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.
Senior Clinical Database Programmer

Senior Clinical Database Programmer

Veristat

Remote

Full-time

Medical, Retirement

Re-posted yesterday


Job description

Job Description:

Senior Clinical Database Programmer

The Senior Clinical Database Programmer will work under the supervision of Principal CDP (or higher-level role) but may work independently as project lead. Working closely with members of Data Management, Statistics, Information Technology (IT), and Quality Control (QC) Departments, the Senior Clinical Database Programmer is responsible for the design and development of electronic and paper Case Report Forms, and to manage, direct, and enable set up of studies using Company's clinical data management systems, including the maintenance and development of computer programs and processes that support team's activities, within scope, budget and timelines in compliance with the United Kingdom Statutory Instrument 2004 No. 1031 and its subsequent amendments, ICH guidelines for Good Clinical Practice and other national and international standards and legislation (as required), Company procedures, and client instructions.

Make an Impact at Veristat!

Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.

  • 105+ approved therapies for marketing applications prepared by Veristat
  • 480+ oncology projects in the past 5 years
  • 350+ rare disease projects delivered in the past 5 years
  • Flexible, inclusive culture - 70% remote workforce, 66% women-led teams

Learn more about our core values here!

What we offer

  • The estimated hiring range for this role is $104K to $115K USD plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to skills and experience, licensure and certifications, education, specific location and dynamic market data.
  • Benefits vary by location and may include:
    • Remote working
    • Flexible time off
    • Paid holidays
    • Medical insurance
    • Tuition reimbursement
    • Retirement plans

What we look for

Bachelor's degree or equivalent (preferred in science) or equivalent work experience.

5-7 years industry and sector experience in eCRF design and development with commercially available CDMS- i.e., Medidata Rave, Oracle InForm/ Central Designer, Veeva, DataLabs, Medrio.

4 years' experience leading eCRF Design/Development/ Maintenance projects and activities without support of a senior colleague.

Able to lead complex studies.

Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.

Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.