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Senior Statistical Programmer Jobs in Washington

Altimmune

Vice President, Biometrics

Gaithersburg, MD · On-site

... programming, and serves as a key partner in shaping cross-functional development plans for ... Serve as the senior statistical representative in regulatory interactions, contributing to briefing ...

Altimmune

Vice President, Biometrics

Gaithersburg, MD · Remote

... programming, and serves as a key partner in shaping cross-functional development plans for ... Serve as the senior statistical representative in regulatory interactions, contributing to briefing ...

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Senior Statistical Programmer information

See Washington salary details

$93.4K

$145.3K

$189.7K

How much do senior statistical programmer jobs pay per year?

As of May 29, 2026, the average yearly pay for senior statistical programmer in Washington 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 is a Senior Statistical Programmer job?

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 key skills and qualifications needed to thrive in the Senior Statistical Programmer position, 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 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.
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Senior Statistical Programmer jobs near you

Senior Specialist Programmer

Fladger Associates

Gaithersburg, MD • On-site

Contractor

Posted 17 days ago

Job description

Gaithersburg, MD
Contract Duration: 12-36 months
Rate: Negotiable

Responsibilities:

  • Excellent employment opportunity for a Senior Specialist Programmer in the Gaithersburg, MD area. (100% remote)
  • The Senior Statistical Programmer is a delivery focused role responsible for programming deliverables with quality and timeliness, following established standards and processes.
  • This position requires high technical skills and thorough industry knowledge to independently perform the programming tasks while using judgement about seeking guidance in complex situations.
  • They can be responsible for leading the programming deliveries of clinical studies or small to medium sized clinical projects and can lead cross-functional teams to deliver continuous improvement
  • Primarily responsible for coordinating the various tools for collecting different types of data.
  • Responsible for ensuring databases are created and adjusted for the end user.
  • Contributes to the development and maintenance of analysis and reporting applications.
  • Able to solve complex problems within own area and will participate in a range of projects.
  • Responsible for leading the programming deliveries of a clinical study or a small to medium sized and complex clinical project
  • Implements statistical programming aspects of the protocol or clinical development program
  • Ensures high quality is built into own deliverables and the quality delivered by other programmers
  • Programs independently with high efficiency and quality
  • Writes specifications and oversee completeness of relevant documentation
  • Contributes to or drives the development of best practices to improve quality, efficiency and effectiveness within function
  • Ensures compliance to standards and automation usage
  • Plans and leads team activities and tasks
  • Identifies, manages and communicates risk within the assigned studies and/or projects
  • Works proactively with study team members including but not limited to the statistician, lead programmer, data manager and study leader
  • Works cooperatively with contract programming providers
  • Influences stakeholders by providing subject matter expertise on programming related items
  • Contributes to or leads technical initiatives
  • Employs Project Management practices in managing programming aspects of drug or technical projects
Experience:
  • Vaccine experience highly desired
  • Bachelor's Degree in Mathematics (i.e., Applied Math, Engineering, etc.), Statistics, Computer Science, Life Science or equivalent
  • 8-10 years of strong Programming experience
    Ability to proactively manage concurrent activities within a study or part of project
  • Excellent programming skills including macro language
  • Proficient knowledge of the clinical development process
  • Thorough knowledge of industry standards
  • Ability to apply Programming knowledge to problem solving
  • Ability to manage relevant documentation
  • Ability to influence relevant stakeholders on Programming related items
  • Ideally candidate would have previous vaccine experience.
  • Ability to proactively manage concurrent activities within a study or part of project