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Sas Statistical Programmer Jobs in Maryland (NOW HIRING)

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... Develop and provide statistical program formats used in the statistical programs (all versions)

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... Develop and provide statistical program formats used in the statistical programs (all versions)

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... Develop and provide statistical program formats used in the statistical programs (all versions)

SAS Programmer

Fort Detrick, MD · On-site

$135K - $148K/yr

Description SAS Programmer Venesco is seeking skilled SAS Programmers to develop validated statistical programs and CDISC-compliant datasets to support clinical trials, statistical analyses, safety ...

SAS Programmer

Frederick, MD · On-site

$135K - $148K/yr

SAS Programmer Venesco is seeking skilled SAS Programmers to develop validated statistical programs and CDISC-compliant datasets to support clinical trials, statistical analyses, safety reporting ...

SAS Programmer Analyst

Baltimore, MD · On-site

$90 - $120/hr

Direct the business process engineering and/or business/user requirements efforts for major ... Experience with statistical modelling tools. * Experience with Data Presentation/Visualization ...

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Sas Statistical Programmer information

See Maryland salary details

$5

$55

$84

How much do sas statistical programmer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for sas statistical programmer in Maryland is $55.68, according to ZipRecruiter salary data. Most workers in this role earn between $20.53 and $82.84 per hour, depending on experience, location, and employer.

What is a SAS statistical programmer?

A SAS Statistical Programmer is a professional who utilizes SAS software to manage, analyze, and report statistical data, primarily in industries like pharmaceuticals, healthcare, and clinical research. They write and validate programs to generate tables, listings, and figures for clinical trials or other data-driven studies. Their role involves ensuring data accuracy, compliance with regulatory guidelines, and collaboration with statisticians and researchers to support decision-making.

What types of projects do SAS statistical programmers typically work on, and how do they collaborate with other teams?

Sas Statistical Programmers often work on projects involving the analysis and reporting of clinical trial or observational study data, producing datasets, tables, listings, and figures to support regulatory submissions or scientific publications. They routinely collaborate with biostatisticians, clinical data managers, and project managers to ensure data quality and compliance with industry standards. Daily responsibilities include coding in SAS, validating datasets, troubleshooting data issues, and preparing documentation. Effective communication and teamwork are essential, as the role frequently involves working in multidisciplinary teams to meet project goals and timelines.

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

To thrive as a Sas Statistical Programmer, you need a strong background in statistics, programming (especially SAS), and data management, usually supported by a degree in statistics, computer science, or a related field. Familiarity with SAS Base, SAS Macro, and clinical data standards like CDISC, as well as relevant industry certifications, are commonly required. Attention to detail, strong problem-solving abilities, and effective communication skills are valuable soft skills. These competencies ensure accurate data analysis, clear reporting, and successful collaboration within cross-functional teams in fields like healthcare or pharmaceuticals.

What job categories do people searching Sas Statistical Programmer jobs in Maryland look for?

The top searched job categories for Sas Statistical Programmer jobs in Maryland are:

What are popular job titles related to Sas Statistical Programmer jobs in MD?

For Sas Statistical Programmer jobs in MD, the most frequently searched job titles are:

Infographic showing various Sas Statistical Programmer job openings in Maryland as of August 2026, with employment types broken down into 93% Full Time, and 7% Contract. Highlights an 86% In-person, and 14% Remote job distribution, with an average salary of $115,817 per year, or $55.7 per hour.

Senior Statistical Programmer

The Emmes Company, LLC

Rockville, MD • On-site

Other

This job post has expired today. Applications are no longer accepted.


Job description

Overview

Senior Statistical Programmer
Be Part of One Team, One Purpose.
At Emmes Group, we're shaping the future of clinical research-where human intelligence meets cutting-edge technology to drive meaningful advancements in healthcare. With over 47 years of scientific excellence, we've led groundbreaking research in cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases, and neuroscience.
Through our two business units-Emmes, a full-service CRO, and Veridix AI, our technology, data, and analytical solutions -we are modernizing clinical trials and accelerating the development of life-changing therapies.
We believe that every clinical breakthrough starts with people-people who are passionate, purpose-driven, and ready to make an impact. At Emmes Group, we bring People, Science, and Technology together to collaborate with our customers and deliver global health impact. Our culture is built on integrity, collaboration, and innovation, ensuring that every challenge is met with perseverance and accountability.
The Senior Statistical Programmer is responsible for programming, validating, and delivering statistical datasets and outputs to support clinical trial analysis and regulatory submissions. Working closely with Biostatistics, Data Management, and Clinical teams, this role contributes to the delivery of high-quality, CDISC-compliant datasets and analysis results for Phase I-IV clinical trials. This position requires strong proficiency in SAS programming, a solid understanding of CDISC standards (SDTM and ADaM), and experience working in a regulated environment.


Responsibilities
  • Programming & Validation
  • Develop, test, and validate SDTM and ADaM datasets according to CDISC standards.
  • Program Tables, Listings, and Figures (TLFs) in support of clinical study reports (CSRs) and regulatory submissions.
  • Translate statistical analysis plans (SAPs) into accurate and efficient code.
  • Project Support
  • Serve as the lead programmer on individual studies or studies within a program.
  • Collaborate with cross functional teams including Biostatisticians, Clinical Data Managers, and Regulatory personnel.
  • Ensure timely and accurate delivery of programming deliverables to support clinical timelines.
  • Quality & Compliance
  • Conduct independent quality checks on programming outputs.
  • Maintain programming documentation according to internal SOPs and regulatory guidelines.
  • Ensure compliance with GCP, ICH, and 21 CFR Part 11 standards.
  • Process Improvement
  • Contribute to the development and refinement of internal programming standards, macros, and reusable code libraries.
  • Identify opportunities to optimize workflows and improve efficiency within the programming team.
  • Performs other duties as assigned
  • Complies with all policies and standards

Qualifications
  • Bachelor's Degree Computer Science, Statistics, Mathematics, Life Sciences, or a related field. Required or
  • Master's Degree Computer Science, Statistics, Mathematics, Life Sciences, or a related field. Preferred
  • 4-6 years as a statistical programmer in a pharmaceutical, biotech, or CRO environment. Required
  • Strong programming skills in SAS as Base, Macro, SQL; familiarity with R or Python is a plus. High
  • In depth knowledge of CDISC SDTM and ADaM standards. High
  • Experience supporting clinical trial reporting and preparing data for regulatory submissions as FDA, EMA. High
  • Excellent attention to detail, problem solving, and communication skills. High
  • Ability to work independently and collaboratively in a fast paced environment. High

If you're looking for a career where your work advances global health and where scientific excellence meets real-world impact, join us and be part of something bigger. One Team, One Purpose.
CONNECT WITH US!
Find us on LinkedIn:/the-emmes-group/
Visit our website:https://www.theemmesgroup.com/


Emmes logo

About Emmes

Sourced by ZipRecruiter

Industry

Scientific research and development services

Company size

201 - 500 Employees

Headquarters location

Rockville, MD, US

Year founded

1977

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