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Entry Level Clinical Sas Programmer Jobs in Kansas

From clinical trials to regulatory, consulting, and market access, every clinical development ... Knowledge of SAS and/or Python is considered an advantage * Familiarity with US and global health ...

... engineering,Cisco routers,Cisco switches,catalyst,meraki Additional Skills & Qualifications ... clinical and business operations Experience Level Entry Level Job Type & Location This is a ...

Entry Level Clinical Sas Programmer information

See Kansas salary details

$17

$48

$71

How much do entry level clinical sas programmer jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for entry level clinical sas programmer in Kansas is $48.19, according to ZipRecruiter salary data. Most workers in this role earn between $37.07 and $60.67 per hour, depending on experience, location, and employer.

What is an entry level clinical SAS programmer?

An Entry Level Clinical SAS Programmer is responsible for programming and analyzing clinical trial data using SAS software. They assist in creating datasets, reports, and statistical outputs that comply with regulatory standards. Their work supports biostatisticians and clinical teams in pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. This role requires knowledge of SAS programming, clinical research processes, and regulatory requirements such as CDISC standards. It is an excellent starting point for those looking to build a career in clinical data analysis and biostatistics.

What are the typical responsibilities of an entry level clinical SAS programmer?

Entry Level Clinical SAS Programmers are primarily responsible for writing and validating SAS code to process clinical trial data, generate tables, listings, and figures, and support statistical analysis plans. They work closely with biostatisticians, data managers, and other team members to ensure data integrity and compliance with regulatory standards. Daily tasks may involve data cleaning, programming data checks, and documenting code for reproducibility. This role offers great exposure to the clinical data lifecycle and provides a strong foundation for professional growth within clinical research and data analytics.

What are the key skills and qualifications needed to thrive as an entry level clinical SAS programmer?

To thrive as an Entry Level Clinical SAS Programmer, you need a solid understanding of SAS programming, statistics, and clinical trial processes, often supported by a degree in computer science, statistics, or a related field. Familiarity with SAS software, data management systems, and FDA or CDISC standards is highly valued, and SAS certification can be a plus. Attention to detail, strong problem-solving skills, and effective communication are key soft skills for this role. These competencies ensure high-quality data analysis, regulatory compliance, and clear collaboration across teams in pharmaceutical or clinical research settings.

What are the most commonly searched types of Clinical Sas Programmer jobs in Kansas?

The most popular types of Clinical Sas Programmer jobs in Kansas are:

What are popular job titles related to Entry Level Clinical Sas Programmer jobs in Kansas?

For Entry Level Clinical Sas Programmer jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Entry Level Clinical Sas Programmer jobs in Kansas look for?

The top searched job categories for Entry Level Clinical Sas Programmer jobs in Kansas are:

What cities in Kansas are hiring for Entry Level Clinical Sas Programmer jobs?

Cities in Kansas with the most Entry Level Clinical Sas Programmer job openings:

Infographic showing various Entry Level Clinical Sas Programmer job openings in Kansas as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 17% Part Time, 1% Temporary, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $100,243 per year, or $48.2 per hour.

Senior RWE Programmer

Parexel

On-site, Remote

Full-time

Posted 28 days ago


Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

30th of 74 rated research


Job description

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Parexel is seeking a Senior Real-World Evidence, RWE Programmer

Join a high-impact team as aremote Sr. Real-World Evidence Programmer,
supporting innovative work. You can work remotely out of Canada or the Continental United States.

If you are passionate about real-world data, advanced analytics,
and delivering meaningful insights, we encourage you to apply.

Who We Are Looking For

  • Effectively designs and codes R and SQL programs
    for assigned project(s), consistently meeting project objectives

  • Expert Coder: The ideal candidate spends most of their time hands-on coding versus project management or oversight responsibilities, has hands-on experience with raw RWE data including both claims data and Flatiron EHR and can write SQL code from scratch.

  • Advanced SQL Programming experience within the Real-World Data (RWD) domain is required.

  • Hands-on experience developing and managing data solutions in the Snowflake platform required.

  • Clean andvalidateReal-World Data (RWD)

  • to ensure consistency and reliability

  • Implement programming based on RWE protocols
    using a variety of RWD sources, including Optum and Flatiron

  • Leverage advanced statistical and epidemiological methodologies
    to deliver robust and reliable analyses

  • Create, review, and approve programming plans
    at both study and project levels

  • Demonstrate advanced knowledge
    of programming, epidemiologicalmethodologyimplementation,
    and system development life cycle concepts

  • Maintain clear documentation
    of analytical programming and operational definitions
    to support reproducible and auditable RWE studies

  • Develop dashboards, reports, and presentations
    to effectively communicate findings

  • Collaborate with study team members
    to meet study timelines and recurring reporting deadlines

What You Will Do

  • Effectively designs and codes R and SQL programs for assigned project(s)
    consistently meetingobjectivesof the project.

  • Daily work % estimates: Coding (80%-90% of their daily work) + copying and pasting the numbers into the excel table shells (5%-20%)

  • Clean and validate RWD
    for consistency and reliability

  • Implement programming as specified from RWE protocol
    using a variety of RWD from multiple sources, including Optum and Flatiron

  • Leverage advanced statistical and epidemiological methodologies
    to deliver robust and reliable analyses

  • Create or review and approve programming plans
    at study and project level.

  • Displays highly advanced knowledgeregardingprogram, epidemiology methodologies implementation
    and system development life cycle concepts.

  • Maintain clear documentation of analytical programming and operational definitions
    to support reproducible and auditable RWE studies

  • Develop dashboards, reports, and presentations
    to communicate findings

  • Work collaboratively with members of study teams
    to meet study and recurring report timelines

Who You Are

  • MS in data science, epidemiology, statistics, public health, or related discipline

  • At least 2-3 years of experience in Real-World Data (RWD) analysis and Real-World Analytics (RWA)using healthcare claims, EMR, and/or registry databases within the biopharmaceutical industry or provider/payer organizations.

  • Hands-on experience with Flatiron datarequired; experience with Optum may be considered

  • Fluency in SQL and R programming isrequired

  • Experience writing original codeand performing raw data analysis (not derived solely from clinical trials)

  • Includes running analyses and/or developing code for real-world analyses

  • Knowledge of SAS and/or Python is considered an advantage

  • Familiarity with US and global healthcare coding systems
    (e.g., ICD, CPT, HCPCS, LOINC, MedDRA)

  • And healthcare delivery systems (e.g., payers and reimbursement models)

  • Experience conducting routine and advanced statistical analyses for RWE generation

  • Including time-to-event, cross-sectional, and longitudinal data

  • Experience with big data analytical platforms

  • Deep understanding of observational study analysis

  • Ability to work independently and contribute to scrum development goals

  • In a fast-paced, flexible, team-oriented environment

  • Strong communicationand collaboration skills

  • Competent in written and oral English.

EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.


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About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983