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Director Statistical Programming Jobs in Washington

Altimmune

Vice President, Biometrics

Gaithersburg, MD · On-site

Direct the development of statistical components of study protocols, statistical analysis plans, and review of statistical programming outputs to ensure accuracy and regulatory readiness * Lead data ...

Altimmune

Vice President, Biometrics

Gaithersburg, MD · Remote

Direct the development of statistical components of study protocols, statistical analysis plans, and review of statistical programming outputs to ensure accuracy and regulatory readiness * Lead data ...

Aledade

Research Scientist

Washington, DC · On-site +1

... direct impact on primary care practices and contributing to a data-driven organization. Primary ... Experience with SQL for data manipulation and R, Python, or Stata for statistical programming.

Tempus

Director, Biostatistics

Triangle, VA

$190K - $260K/yr

The Director of Biostatistics builds and maintains strong collaborations with other teams across ... Experience working with other groups involved in clinical research, such as Statistical Programmers ...

Aledade

Research Scientist

Washington, DC · Remote

... direct impact on primary care practices and contributing to a data-driven organization. Primary ... Experience with SQL for data manipulation and R, Python, or Stata for statistical programming.

Aledade

Research Scientist

Washington, DC

... direct impact on primary care practices and contributing to a data-driven organization. Primary ... Experience with SQL for data manipulation and R, Python, or Stata for statistical programming.

Pewtrusts

Research Methodologist

Washington, DC · Hybrid

$110K/yr

The Research Methodologist reports to the Associate Director for U.S. Survey Methods and works ... Strong proficiency programming in the R statistical programming language is required. (Beginner ...

Captivation Software

Test Engineer 3

Annapolis, MD · On-site

$130K - $270K/yr

Bachelor's degree in Math, Science, Engineering, Statistics, Engineering Management or related ... This position is open for direct hires only. We will not consider candidates from third party ...

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Director Statistical Programming information

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$173.9K

$317.3K

$389.6K

How much do director statistical programming jobs pay per year?

As of May 31, 2026, the average yearly pay for director statistical programming in Washington is $317,294.00, according to ZipRecruiter salary data. Most workers in this role earn between $295,000.00 and $365,300.00 per year, depending on experience, location, and employer.

What Is the Job of a Director Statistical Programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

What are the key skills and qualifications needed to thrive as a Director of Statistical Programming, and why are they important?

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

How does a Director of Statistical Programming typically collaborate with cross-functional teams in a pharmaceutical or biotech company?

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.

What does a Director of Statistical Programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.
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Director Statistical Programming jobs near you
Infographic showing various Director Statistical Programming job openings in Washington as of May 2026, with employment types broken down into 7% As Needed, 76% Full Time, 14% Part Time, 2% Contract, and 1% Summer. Highlights an 74% Physical, 8% Hybrid, and 18% Remote job distribution, with an average salary of $317,294 per year, or $152.5 per hour.
Vice President, Biometrics

Vice President, Biometrics

Altimmune

Gaithersburg, MD • On-site

Full-time

Posted 25 days ago

Job description

About Altimmune:
Altimmune (NASDAQ: ALT) is a late clinical-stage biopharmaceutical company developing therapies for patients with serious liver diseases. The Company's lead candidate, pemvidutide, is a unique dual-action therapy targeting both glucagon and GLP-1 receptors in a balanced 1:1 ratio in development for the treatment of metabolic dysfunction-associated steatohepatitis (MASH), alcohol use disorder (AUD), and alcohol-associated liver disease (ALD). For more information, please visit .
Summary of Position:
Reporting to the Chief Medical Officer, the Vice President of Biometrics provides strategic leadership and oversight for all statistical and data management activities supporting Altimmune's clinical development portfolio. This role defines and drives the statistical strategy for programs from early development through pivotal trials and regulatory submission - and in the future will drive real-world evidence generation and post-marketing activities - ensuring the scientific integrity of clinical trial design, analysis, and interpretation. The Vice President, Biometrics, oversees internal and external teams across biostatistics, data management, and statistical programming, and serves as a key partner in shaping cross-functional development plans for pemvidutide in MASH, AUD, and ALD. The position plays a central role in quantitative decision-making, regulatory interactions, and the application of statistical methodologies. Success requires exceptional scientific judgment, a strong regulatory track record, and the ability to communicate complex statistical concepts early across clinical, scientific, and executive stakeholders. Depending upon location, this role will be hybrid or remote and will require some travel as business needs dictate.
Essential Functions:
  • Shape statistical strategy for clinical development programs, including endpoint selection, estimand frameworks, and overall statistical positioning to support program objectives and corporate milestones
  • Evaluate, recommend, and implement innovative statistical techniques - including adaptive designs, Bayesian methods, enrichment strategies, and real-world evidence integration - to enhance trial efficiency and decision-making
  • Contribute to portfolio-level planning, including scenario modeling, probability of success assessments, quantitative risk evaluation, and go/no-go recommendations
  • Oversee the development and governance of standard processes, systems, and infrastructure for biometrics, data management, and statistical analysis programming to ensure quality, consistency, and compliance
  • Direct the development of statistical components of study protocols, statistical analysis plans, and review of statistical programming outputs to ensure accuracy and regulatory readiness
  • Lead data collection, validation, management, and storage strategies that meet data standards and support high-quality regulatory submissions
  • Serve as the senior statistical representative in regulatory interactions, contributing to briefing packages, responses, and advisory committee preparation
  • Lead, mentor, and develop a high-performing biostatistics and data management team, fostering scientific excellence, accountability, and cross-functional collaboration
  • Manage external partners and CROs to ensure high-quality, timely deliverables and alignment with internal standards and program needs
  • Ensures timely and accurate delivery of clinical study data analyses to support program decisions, regulatory filings, and communication
  • Interpret and communicate clinical trial data to internal and external stakeholders, contributing to scientific publications, presentations, and regulatory submission documents

Job Requirements (Essential knowledge, skills, and attributes):
  • MS or PhD in Biostatistics, Statistics, or related quantitative field
  • 15 or more years of industry experience in biotech or pharma
  • At least 8 years' experience leading and developing high-performing teams
  • Demonstrated success leading statistical strategy for pivotal trials and significant contributions to successful regulatory submissions (IND, NDA, BLA, MAA), with a strong track record of direct interaction with global health authorities.
  • Proven ability to lead and scale teams, including remote and in-person teams
  • Strong communication skills, both orally and in writing, with an ability to interpret and communicate statistical concepts and results clearly to non-statistical stakeholders, senior executives, investigators, vendors, and regulatory agencies.
  • Deep expertise in clinical trial design and statistical methodology across all phases, including confirmatory trial methods, multiplicity control, missing data strategies, interim monitoring, estimand-aligned analyses, and benefit-risk assessment
  • Experience with innovative and complex designs such as adaptive trials, Bayesian methods, enrichment strategies, and integration of real-world evidence
  • Familiarity with modern data infrastructure, including CDISC standards, data visualization tools, and statistical programming environments; proficiency with SAS for complex analyses
  • Proven ability to operate effectively in fast-paced, entrepreneurial biotech settings, balancing scientific rigor with practical decision-making
  • History of successful collaboration in a team environment throughout the organization, with strong organizational skills and the ability to prioritize multiple competing demands
  • Experience with Data Monitoring Committees and therapeutic experience in metabolic diseases preferred but not required.

Altimmune provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

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