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Senior Statistical Programmer Analyst Jobs in Washington, DC

Senior Programmer Analyst

Rockville, MD · On-site

$45.50 - $61.50/hr

The Senior Programmer may also provide programming and statistical analysis services using MEPS and HCUP data using econometric and statistical techniques used with a variety of large data sources ...

Senior programmers work closely with other programmers, analysts, IT staff, and managers to understand system needs and develop solutions within set timelines and budgets. A senior programmer should ...

Senior Programmer Analyst

Suitland, MD · On-site

$100 - $125/hr

Overview/ Job Responsibilities We are looking for a Senior Programmer Analyst to join a team of twenty software/system/network specialists supporting the operations and maintenance of the ground ...

We are looking for a Senior Programmer Analyst to join a team of twenty software/system/network specialists supporting the operations and maintenance of the ground systems for NOAA's environmental ...

Senior Programmer Analyst

Suitland, MD · On-site

$100K - $125K/yr

Overview/ Job Responsibilities We are looking for a Senior Programmer Analyst to join a team of twenty software/system/network specialists supporting the operations and maintenance of the ground ...

Senior Programmer Analyst

Suitland, MD · On-site

$100K - $125K/yr

Overview/ Job Responsibilities We are looking for a Senior Programmer Analyst to join a team of twenty software/system/network specialists supporting the operations and maintenance of the ground ...

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Showing results 1-20

Senior Statistical Programmer Analyst information

See Washington, DC salary details

$93.4K

$145.3K

$189.7K

How much do senior statistical programmer analyst jobs pay per year?

As of Aug 28, 2026, the average yearly pay for senior statistical programmer analyst in Washington, DC is $145,305.00, according to ZipRecruiter salary data. Most workers in this role earn between $121,200.00 and $167,600.00 per year, depending on experience, location, and employer.

What does a senior statistical programmer analyst do?

A Senior Statistical Programmer Analyst is responsible for designing, developing, and validating statistical programs that analyze clinical trial or research data. They work closely with biostatisticians and data managers to ensure data accuracy, integrity, and compliance with regulatory standards. Their work includes creating tables, listings, and figures (TLFs), developing analysis datasets, and automating data processes. Senior Statistical Programmer Analysts often mentor junior programmers and play a key role in quality control and project delivery within pharmaceutical, biotechnology, or clinical research organizations.

How does a senior statistical programmer analyst typically collaborate with cross-functional teams in clinical research projects?

As a Senior Statistical Programmer Analyst, you will regularly collaborate with biostatisticians, data managers, clinical research associates, and project managers. Your main responsibility is to translate statistical analysis plans into programming code (often using SAS or R), ensuring datasets and outputs meet regulatory standards. You’ll participate in team meetings to clarify study requirements, address data or programming issues, and ensure timelines are met. Strong communication and documentation skills are essential, as you often serve as a bridge between technical and non-technical team members.

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

To thrive as a Senior Statistical Programmer Analyst, you need advanced programming skills in SAS or R, a strong background in statistics, and a relevant degree such as in mathematics, statistics, or computer science. Experience with clinical trial data, CDISC standards (SDTM, ADaM), and regulatory submission processes, along with certifications like SAS Certified Professional, are highly valued. Exceptional problem-solving abilities, attention to detail, and effective communication enable you to manage complex datasets and collaborate with cross-functional teams. These combined skills ensure accurate data analysis, regulatory compliance, and successful delivery of biostatistical projects in the pharmaceutical or clinical research industry.

What are popular job titles related to Senior Statistical Programmer Analyst jobs in Washington, DC?

For Senior Statistical Programmer Analyst jobs in Washington, DC, the most frequently searched job titles are:

What job categories do people searching Senior Statistical Programmer Analyst jobs in Washington, DC look for?

The top searched job categories for Senior Statistical Programmer Analyst jobs in Washington, DC are:

Infographic showing various Senior Statistical Programmer Analyst job openings in Washington, DC as of August 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 79% In-person, 3% Hybrid, and 18% Remote job distribution, with an average salary of $145,305 per year, or $69.9 per hour.

Senior Statistical Programmer

The Emmes Company, LLC

Rockville, MD • On-site

Other

Posted 8 days ago


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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