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Entry Level Clinical Sas Programmer Jobs (NOW HIRING)

... clinical reporting, verification and submissions support. About the Role * Independently, perform SAS programming and analysis support of the generation of analysis datasets, statistical analysis ...

Broad experience across a range of clinical and nonclinical projects and demonstrated support of diverse client needs. * Demonstrated management and leadership skills. * Skilled SAS programming ...

This role requires strong proficiency in R and/or SAS and understanding of clinical trial processes ... Conduct programming peer reviews, provide technical guidance, and mentor junior programmers to ...

This role requires strong proficiency in R and/or SAS and understanding of clinical trial processes ... Conduct programming peer reviews, provide technical guidance, and mentor junior programmers to ...

Company Description Coders Data is an incorporated consulting team of designers, developers, and ... SAS Analyst is the most efficient data analyst in the world built to facilitate mining, altering ...

Company Description Coders Data is an incorporated consulting team of designers, developers, and ... SAS Analyst is the most efficient data analyst in the world built to facilitate mining, altering ...

... SAS Macros. * The Programmer will: - Consolidate heterogeneous data sources (e.g. clinical study databases, external databases, real-world data) to prepare analysis-ready data sets within a defined ...

Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research * Expert knowledge and understanding of the SAS programming * Expert ...

... SAS Macros. * The Programmer will: - Consolidate heterogeneous data sources (e.g. clinical study databases, external databases, real-world data) to prepare analysis-ready data sets within a defined ...

Principal Statistician

Durham, NC · On-site

$110 - $150/hr

Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research * Expert knowledge and understanding of the SAS programming * Expert ...

Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research * Expert knowledge and understanding of the SAS programming * Expert ...

Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research * Expert knowledge and understanding of the SAS programming * Expert ...

Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research * Expert knowledge and understanding of the SAS programming * Expert ...

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Entry Level Clinical Sas Programmer information

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

As of Aug 23, 2026, the average hourly pay for entry level clinical sas programmer in the United States is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $68.03 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.

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Infographic showing various Entry Level Clinical Sas Programmer job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $112,399 per year, or $54 per hour.

Full-time

Re-posted 5 days ago


Job description

Role: Statistical Programmer II
Location : Tampa, Florida
Job Duties:
Roles and responsibilities she perfomed as a Statistical Programmer I/ Sas Programmer I from
Sep2019 - Jan2021 Includes the follows:
Provide statistical programming support for the reporting of clinical trial results of Phase 1
and Phase 2
Experience working with systems used within the Clinical Trial process.
Generated program as per STDM standards and Documentation of SAS code, log, Output
and report as per SOP guidelines.
Performed CDISC Mapping for Ongoing clinical trials and classified data into domains.
understanding with CDISC SDTM Implementation Guide v3.1.2/ v3.1.3 and SDTM
Model.
Proficient in generating clinical reports for safety analysis in the form of tables and listings.
Developed reports for safety as per study requirements debugging SAS errors and
identifying issues producing reports or analysis data sets and SAS data sets.
Roles and responsibilities she perfomed as a Statistical Programmer II/ Sas Programmer II from
feb2021 - Dec2022 Includes the follows:
Experienced in Writing statistical programs using SAS and R as per requests from internal
or external clients and reviewing the statistical analysis plan (SAP), SDRG and ADRG.
Handling of multiple Projects of client data to analyze Phase II and Phase III Clinical trials
data in various therapeutic areas like Hematology, endocrinology, Dermatology,
Gastroenterology, Immunology, Neurology and Virology to provide statistical
programming by using SAS tools such as SAS/MACROS, SAS/SQL and R experience for
the reporting of clinical trial results.
Involved in error handling, fixing bugs, and overcoming the challenges faced while
developing the code of specified structure of Tables and listings through creating Macros
and macro variables.
Experienced in data validation and data cleaning and worked understanding with CDISC
SDTM Implementation Guide v3.2/v3.3 and SDTM Model checks (through specifications) on
clinical trial datasets and QC of Statistical/ Programming outputs like Analysis Datasets and
aCRF (Case Report Form).
Experienced in creating reports using proc report and derived data sets (SDTM, CDISC,
ADAM) and Generated Define.xml output for FDA regulatory submissions.
Created efficacy customize reports for FDA regulatory submissions and develop to
maintain SAS programs to create SDTM and Adam datasets and created Tables and
Figures to support clinical trials.
Track clinical trial milestones for statistical programming deliverables.
Ensure compliance with SOPs/Guidelines, ICH-GCP, and any other applicable local and
international regulations, and participate in internal/external audits and regulatory
inspections as required.
Analyzed and validated data sets and SAS outputs with other programmer's outputs and
mockups in SAP using PROC COMPARE, PROC CONTENTS and PROC FREQ. Created
formats for the coded data and used PROC SQL for data validation.