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$90.6K

$157.9K

$266.9K

How much do statistical programmer jobs pay per year?

As of Aug 21, 2026, the average yearly pay for statistical programmer in Bethesda, MD is $157,857.00, according to ZipRecruiter salary data. Most workers in this role earn between $134,000.00 and $171,500.00 per year, depending on experience, location, and employer.

What is a statistical programmer?

Statistical programmers are professionals who use statistical software and programming languages, such as SAS, R, or Python, to manage, analyze, and report data, often in clinical trials, public health, or research settings. They play a crucial role in transforming raw data into meaningful results by writing code for data cleaning, data manipulation, statistical analysis, and generating reports. Statistical programmers often work closely with statisticians, data managers, and researchers to ensure the accuracy and integrity of data analyses. Their work is essential in industries like pharmaceuticals, healthcare, and academia.

What does a statistical programmer do?

A statistical programmer creates statistical programming deliverables. You ensure excellent programming of analysis-ready data, tables, and figures. You may use Stata for general purpose statistical analysis or SPSS for interactive or batched statistical analysis. Your responsibilities include developing standard operating procedures and complying with guidelines. Other duties include remaining informed on developments in programming standards and meeting all regulatory requirements. You also create PROC statements that call upon named procedures for analysis. You develop programs for dataset integration, prepare resource plans, and assist with quality control of datasets.

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

To thrive as a Statistical Programmer, you need a strong background in statistics, data analysis, and programming—typically with a degree in statistics, mathematics, computer science, or a related field. Expertise in statistical software such as SAS, R, or Python and familiarity with data management systems like CDISC or SQL are often required, along with relevant certifications. Strong problem-solving abilities, attention to detail, and clear communication skills help you interpret data accurately and collaborate effectively with cross-functional teams. These skills ensure the delivery of high-quality, reproducible statistical analyses crucial for informed decision-making in research and industry settings.

What are some common challenges faced by statistical programmers when working on clinical trial data?

Statistical Programmers often encounter challenges such as managing large, complex datasets, ensuring data integrity, and adhering strictly to regulatory standards (like CDISC SDTM and ADaM). They must also collaborate closely with biostatisticians and data managers to accurately translate statistical analysis plans into code. Tight project timelines and shifting priorities can require strong organizational skills and adaptability. Effective communication and attention to detail are essential for navigating these challenges and delivering reliable results.

What is the difference between Statistical Programmer vs Data Analyst?

AspectStatistical ProgrammerData Analyst
Required CredentialsBachelor's in Statistics, Biostatistics, or related field; experience with SAS, R, or PythonBachelor's in Statistics, Data Science, or related field; proficiency in Excel, SQL, and visualization tools
Work EnvironmentPharmaceutical, clinical research, or healthcare industries; focus on programming and data managementVarious industries including finance, marketing, healthcare; focus on data interpretation and reporting
Employer & Industry UsageCommon in clinical trials, biotech, pharma companiesUsed across multiple sectors like finance, retail, and healthcare

While both roles handle data, Statistical Programmers primarily focus on programming and managing clinical or research data, whereas Data Analysts interpret data to generate insights across various industries. The roles often overlap in skills like statistical software proficiency but differ in their core responsibilities and industry focus.

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Statistical Programmer jobs near you
Infographic showing various Statistical Programmer job openings in Bethesda, MD as of August 2026, with employment types broken down into 1% Internship, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $157,857 per year, or $75.9 per hour.

Senior Statistical Programmer

The Emmes Company, LLC

Rockville, MD • On-site

Other

Posted yesterday

New

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/

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About Emmes

Sourced by ZipRecruiter

Industry

Scientific research and development services

Company size

201 - 500 Employees

Headquarters location

Rockville, MD, US

Year founded

1977

Social media

Twitter

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