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Statistical Programmer Jobs in Brooklyn, NY (NOW HIRING)

2T Consulting

Senior Statistical Analyst

Brooklyn, NY · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...

2T Consulting

Senior Statistical Analyst

Hoboken, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...

2T Consulting

Senior Statistical Analyst

Pelham, NY · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...

2T Consulting

Senior Statistical Analyst

Elmhurst, NY · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...

2T Consulting

Senior Statistical Analyst

Nutley, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...

2T Consulting

Senior Statistical Analyst

Woodhaven, NY · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...

2T Consulting

Senior Statistical Analyst

Haworth, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...

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All JobsStatistical Programmer JobsStatistical Programmer Jobs in Brooklyn, NY

Statistical Programmer information

See Brooklyn, NY salary details

$88.9K

$154.9K

$261.8K

How much do statistical programmer jobs pay per year?

As of Sep 5, 2026, the average yearly pay for statistical programmer in Brooklyn, NY is $154,878.00, according to ZipRecruiter salary data. Most workers in this role earn between $131,400.00 and $168,200.00 per year, depending on experience, location, and employer.

What is a statistical programmer?

Statistical programmers are professionals who use statistical software and programming languages, such as SAS, R, or Python, to manage, analyze, and report data, often in clinical trials, public health, or research settings. They play a crucial role in transforming raw data into meaningful results by writing code for data cleaning, data manipulation, statistical analysis, and generating reports. Statistical programmers often work closely with statisticians, data managers, and researchers to ensure the accuracy and integrity of data analyses. Their work is essential in industries like pharmaceuticals, healthcare, and academia.

What does a statistical programmer do?

A statistical programmer creates statistical programming deliverables. You ensure excellent programming of analysis-ready data, tables, and figures. You may use Stata for general purpose statistical analysis or SPSS for interactive or batched statistical analysis. Your responsibilities include developing standard operating procedures and complying with guidelines. Other duties include remaining informed on developments in programming standards and meeting all regulatory requirements. You also create PROC statements that call upon named procedures for analysis. You develop programs for dataset integration, prepare resource plans, and assist with quality control of datasets.

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

To thrive as a Statistical Programmer, you need a strong background in statistics, data analysis, and programming—typically with a degree in statistics, mathematics, computer science, or a related field. Expertise in statistical software such as SAS, R, or Python and familiarity with data management systems like CDISC or SQL are often required, along with relevant certifications. Strong problem-solving abilities, attention to detail, and clear communication skills help you interpret data accurately and collaborate effectively with cross-functional teams. These skills ensure the delivery of high-quality, reproducible statistical analyses crucial for informed decision-making in research and industry settings.

What are some common challenges faced by statistical programmers when working on clinical trial data?

Statistical Programmers often encounter challenges such as managing large, complex datasets, ensuring data integrity, and adhering strictly to regulatory standards (like CDISC SDTM and ADaM). They must also collaborate closely with biostatisticians and data managers to accurately translate statistical analysis plans into code. Tight project timelines and shifting priorities can require strong organizational skills and adaptability. Effective communication and attention to detail are essential for navigating these challenges and delivering reliable results.

What is the difference between Statistical Programmer vs Data Analyst?

AspectStatistical ProgrammerData Analyst
Required CredentialsBachelor's in Statistics, Biostatistics, or related field; experience with SAS, R, or PythonBachelor's in Statistics, Data Science, or related field; proficiency in Excel, SQL, and visualization tools
Work EnvironmentPharmaceutical, clinical research, or healthcare industries; focus on programming and data managementVarious industries including finance, marketing, healthcare; focus on data interpretation and reporting
Employer & Industry UsageCommon in clinical trials, biotech, pharma companiesUsed across multiple sectors like finance, retail, and healthcare

While both roles handle data, Statistical Programmers primarily focus on programming and managing clinical or research data, whereas Data Analysts interpret data to generate insights across various industries. The roles often overlap in skills like statistical software proficiency but differ in their core responsibilities and industry focus.

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Cities near Brooklyn, NY with the most Statistical Programmer job openings:

Statistical Programmer jobs near you
Infographic showing various Statistical Programmer job openings in Brooklyn, NY as of August 2026, with employment types broken down into 1% Internship, 87% Full Time, 10% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $154,878 per year, or $74.5 per hour.

Contractor - Principal Statistical Programmer

Syndax Pharmaceuticals

New York, NY • On-site

Full-time

Posted 15 days ago

Key responsibilities

  • Support study leads and take ownership of multiple deliverables within a drug program.

  • Serve as a primary programmer for the production of tables, listings, figures, and CRF tabulations for clinical trial programs.

  • Troubleshoot and review complex SAS programs, ensuring quality and adherence to good programming practices.

Job description

Syndax Pharmaceuticals is looking for a Contractor - Principal Statistical Programmer
At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies.
The Role:
The Principal Statistical Programmer will provide expert-level hands-on programming support and technical expertise to develop, maintain, validate, and execute SAS programs that access, visualize, analyze, and report clinical trial data in accordance with statistical analysis plans, ICH guidelines, and applicable regulatory requirements. The Principal Statistical Programmer performs the statistical programming required for analysis of clinical trial data on projects for in-house and out-sourced clinical trials, commercial requests, Health Economics Outcome Research (HEOR) analyses, pooled analysis such as integrated summary of efficacy (ISE) and integrated summary of safety (ISS) and any ad-hoc analyses as required.
The candidate will have a proven ability to work independently, possess excellent communication skills, and have advanced expertise in SAS programming.
Key Responsibilities:
  • Supports study leads and take ownership of multiple deliverables within a drug program whilst providing support across various drug platforms.
  • Acts as an integral member of project team, complementing the lead programmer as required. May attend project team meetings as required and will cross-collaborate with vendors, biostatisticians, data managers, and other cross-functional teams as required.
  • Serve in a primary role for production of all tables, listings, and figures, and Case Report Form (CRF) tabulations for clinical trial programs including ISS/ISE.
  • Serve as a primary programmer to support regulatory requests, commercial requests, ad hoc analyses, biomarker analyses, HEOR analyses etc.
  • May review critical Standards Artifacts and Processes (such as Statistical Analysis Plans, Data Validation Plans, eCRFs, etc.) and provide constructive comments.
  • Troubleshoots and provides quality review of complex SAS programs.
  • Follows good programming practices and adequately documents programs.
  • Understands and follows FDA regulations which affect the reporting of clinical trial data.
  • May participate in cross functional task forces and initiatives representing Statistical Programming.

Desired Experience/Education and Personal Attributes:
  • At least eight years of relevant experience. Exceptional candidates with 5+ years of experience may be considered.
  • Bachelor's degree.
  • Experience in Oncology required; Leukemia experience preferred.
  • Ability to communicate technical concepts clearly and concisely to non-technical colleagues.
  • Successfully completed several large or complex projects.
  • Ability to handle multiple projects with aggressive timelines.
  • Ability to multitask and prioritize work.
  • Excellent knowledge of SAS.
  • Familiarity with coding dictionaries (WHO, MedDRA).
  • Expert at industry standard initiatives such as CDISC.
  • Knowledge of medical and statistical terminology.
  • Capable of using Windows, Word, and Excel.

Location: While our corporate headquarters are located in New York City, this position is open to candidates from any location with a preference for east coast locations.
About Syndax:
Syndax Pharmaceuticals is a commercial-stage biopharmaceutical company advancing innovative cancer therapies. Highlights of the Company's pipeline include a menin inhibitor for R/R acute leukemia and a monoclonal antibody that blocks the CSF-1 receptor for chronic graft-versus-host disease. Fueled by our commitment to reimagining cancer care, Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment. For more information, please visit www.syndax.com/ or follow the Company on X and LinkedIn.
Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
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