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Statistical Programmer 1 Jobs in Washington (NOW HIRING)

Capital One

Sr. Business Analyst

Mclean, VA · On-site

$93K - $120K/yr

Master's Degree in Business or quantitative field such as Finance, Economics, Physical Sciences, Math, Statistics, Engineering * 1+ years of experience in Statistical model building * 1+ years of ...

Capital One

Sr. Business Analyst - US Card

Mclean, VA · On-site

$93K - $120K/yr

Master's Degree in Business or quantitative field such as Finance, Economics, Physical Sciences, Math, Statistics, Engineering * 1+ years of experience in Statistical model building * 1+ years of ...

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Statistical Programmer 1 information

What is a statistical programmer 1?

Statistical Programmers are professionals who use specialized software and programming languages, such as SAS, R, or Python, to manage, analyze, and report on data—often in clinical research, pharmaceuticals, or healthcare settings. They work closely with statisticians and data managers to ensure data accuracy, create statistical tables, and support the analysis of clinical trials or research studies. Statistical Programmers play a key role in transforming raw data into meaningful results that inform scientific and regulatory decisions.

What are the key skills and qualifications needed to thrive as a statistical programmer 1?

To thrive as a Statistical Programmer 1, you need a solid background in statistics or mathematics, programming proficiency (especially in SAS or R), and a relevant bachelor's degree. Familiarity with data management tools, clinical trial data standards (such as CDISC), and statistical analysis software is typically required. Attention to detail, problem-solving skills, and effective communication help you accurately interpret data and collaborate with cross-functional teams. These competencies are crucial for ensuring data integrity, meeting regulatory requirements, and delivering high-quality statistical outputs in clinical research environments.

What are common challenges faced by statistical programmer 1s when working with clinical trial data?

Statistical Programmer 1s often encounter challenges such as managing large and complex datasets, ensuring data integrity, and adhering to strict regulatory standards like CDISC and FDA requirements. They must also communicate closely with biostatisticians and data managers to clarify analysis needs and address data discrepancies. Balancing multiple projects with tight deadlines while maintaining accurate and reproducible code is another frequent challenge, making organizational skills and attention to detail essential in this role.

What is the difference between Statistical Programmer 1 vs Statistical Programmer 2?

AspectStatistical Programmer 1Statistical Programmer 2
Required CredentialsBachelor's degree in statistics, biostatistics, or related fieldBachelor's or master's degree, with more experience
Work EnvironmentEntry-level, supporting clinical trial data analysisMore independent, handling complex datasets
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsSame as Statistical Programmer 1, with increased responsibilities
Common Search & ComparisonYesYes

The main difference between Statistical Programmer 1 and Statistical Programmer 2 lies in experience and responsibility. Statistical Programmer 2 typically has more experience, handles more complex tasks, and works more independently. Both roles are common in the pharmaceutical and biotech industries, often requiring similar educational backgrounds, but Statistical Programmer 2 is expected to take on greater responsibilities.

What are popular job titles related to Statistical Programmer 1 jobs in Washington?

For Statistical Programmer 1 jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Statistical Programmer 1 jobs in Washington look for?

The top searched job categories for Statistical Programmer 1 jobs in Washington are:

Statistical Programmer 1 jobs near you
Infographic showing various Statistical Programmer 1 job openings in Washington as of August 2026, with employment types broken down into 2% Internship, 83% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution.

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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