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Senior Statistical Programmer Jobs in Laurel, MD

Econometrica

Senior SAS/Python Programmer

Bethesda, MD · On-site +1

Job Title Senior SAS/Python Programmer Job Type Full-time Location Bethesda Office - Bethesda, MD ... The candidate will work alongside a multidisciplinary team of statistical programmers, data ...

New

Ra

Marketing Analytics Senior Manager

Washington, DC · On-site

Senior Level This is what you will do.. You will be using quantitative methods to assess the impact ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

Via Logic LLC

Senior AI Engineer

Rockville, MD · On-site

$130 - $160/hr

As a Senior AI Engineer, you will * Support the development and operationalization of AI and ... Apply cutting‑edge techniques in statistical analysis, predictive analytics, entity resolution ...

Elder Research

Senior Data Engineer

Arlington, VA · Hybrid

$121K - $165K/yr

Senior Data Engineer General Information Requisition # 683 Locations USA-VA-Arlington Posting Date ... Bachelor of Science degree in a relevant field such as statistics, computer science, economics ...

Elder Research

Senior Data Engineer

Arlington, VA · On-site

$121K - $165K/yr

Senior Data Engineer General Information Requisition # 683 Locations USA-VA-Arlington Posting Date ... Bachelor of Science degree in a relevant field such as statistics, computer science, economics ...

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Senior Statistical Programmer information

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$81.8K

$127.2K

$166.1K

How much do senior statistical programmer jobs pay per year?

As of Aug 30, 2026, the average yearly pay for senior statistical programmer in Laurel, MD is $127,198.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,100.00 and $146,700.00 per year, depending on experience, location, and employer.

What is a senior statistical programmer?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

What are the typical responsibilities and team dynamics for a senior statistical programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.

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

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

What are popular job titles related to Senior Statistical Programmer jobs in Laurel, MD?

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

What cities near Laurel, MD are hiring for Senior Statistical Programmer jobs?

Cities near Laurel, MD with the most Senior Statistical Programmer job openings:

Senior Statistical Programmer jobs near you
Infographic showing various Senior Statistical Programmer job openings in Laurel, MD as of August 2026, with employment types broken down into 1% Internship, 81% Full Time, 16% Part Time, and 2% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $127,198 per year, or $61.2 per hour.

Senior Statistical Programmer

Rockville, MD • On-site

The Emmes Company, LLC
Scientific Research and Development Services • 201 - 500 employees
Learn more about The Emmes Company, LLCexternal

Other

Posted 9 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/

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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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