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 ...
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 ...
Network Engineer
$45 - $65/hr
... engineering,Cisco routers,Cisco switches,catalyst,meraki Additional Skills & Qualifications ... clinical and business operations Experience Level Entry Level Job Type & Location This is a ...
Network Engineer
$45 - $65/hr
... engineering,Cisco routers,Cisco switches,catalyst,meraki Additional Skills & Qualifications ... clinical and business operations Experience Level Entry Level Job Type & Location This is a ...
Associate Sales Representative, CRM (Wichita, KS)
$43K - $109K/yr
Provides engineering, sales, education, and clinical support in response to field inquiries on as ... Utilized as entry level role for those coming in outside of the CA Associate program with minimum ...
Associate Sales Representative, CRM (Wichita, KS)
$43K - $109K/yr
Provides engineering, sales, education, and clinical support in response to field inquiries on as ... Utilized as entry level role for those coming in outside of the CA Associate program with minimum ...
Associate Sales Representative, CRM (Wichita, KS)
Wichita, KS · On-site
$43K - $109K/yr
Provides engineering, sales, education, and clinical support in response to field inquiries on as ... Utilized as entry level role for those coming in outside of the CA Associate program with minimum ...
Associate Sales Representative, CRM (Wichita, KS)
Wichita, KS · On-site
$43K - $109K/yr
Provides engineering, sales, education, and clinical support in response to field inquiries on as ... Utilized as entry level role for those coming in outside of the CA Associate program with minimum ...
Associate Sales Representative, CRM (Wichita, KS)
Wichita, KS · On-site
$43K - $109K/yr
Provides engineering, sales, education, and clinical support in response to field inquiries on as ... Utilized as entry level role for those coming in outside of the CA Associate program with minimum ...
Associate Sales Representative, CRM (Wichita, KS)
Wichita, KS · On-site
$43K - $109K/yr
Provides engineering, sales, education, and clinical support in response to field inquiries on as ... Utilized as entry level role for those coming in outside of the CA Associate program with minimum ...
Entry Level Clinical Sas Programmer information
See Kansas salary details
$17.15 - $22.10
4% of jobs
$22.10 - $27.05
9% of jobs
$27.05 - $32
4% of jobs
$32 - $36.95
7% of jobs
$37.26 is the 25th percentile. Wages below this are outliers.
$36.95 - $41.90
9% of jobs
The median wage is $46.85 / hr.
$41.90 - $46.85
17% of jobs
$46.85 - $51.80
7% of jobs
$51.80 - $56.75
14% of jobs
$58.33 is the 75th percentile. Wages above this are outliers.
$56.75 - $61.70
12% of jobs
$61.70 - $66.66
10% of jobs
$66.66 - $71.61
7% of jobs
$17
$48
$71
How much do entry level clinical sas programmer jobs pay per hour?
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:

Parexel rating
8.2
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 objectivesExpert 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.
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