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Senior Statistical Programmer Analyst Jobs (NOW HIRING)

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

Arverne, 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

Garfield, 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

Corona, 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

Maywood, 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

Hillside, 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

Carlstadt, 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

Wood Ridge, 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

Yonkers, 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

Closter, 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

Maplewood, 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

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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Senior Statistical Programmer Analyst information

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$82.5K

$128.3K

$167.5K

How much do senior statistical programmer analyst jobs pay per year?

As of Aug 21, 2026, the average yearly pay for senior statistical programmer analyst in the United States is $128,293.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,000.00 and $148,000.00 per year, depending on experience, location, and employer.

What does a senior statistical programmer analyst do?

A Senior Statistical Programmer Analyst is responsible for designing, developing, and validating statistical programs that analyze clinical trial or research data. They work closely with biostatisticians and data managers to ensure data accuracy, integrity, and compliance with regulatory standards. Their work includes creating tables, listings, and figures (TLFs), developing analysis datasets, and automating data processes. Senior Statistical Programmer Analysts often mentor junior programmers and play a key role in quality control and project delivery within pharmaceutical, biotechnology, or clinical research organizations.

How does a senior statistical programmer analyst typically collaborate with cross-functional teams in clinical research projects?

As a Senior Statistical Programmer Analyst, you will regularly collaborate with biostatisticians, data managers, clinical research associates, and project managers. Your main responsibility is to translate statistical analysis plans into programming code (often using SAS or R), ensuring datasets and outputs meet regulatory standards. You’ll participate in team meetings to clarify study requirements, address data or programming issues, and ensure timelines are met. Strong communication and documentation skills are essential, as you often serve as a bridge between technical and non-technical team members.

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

To thrive as a Senior Statistical Programmer Analyst, you need advanced programming skills in SAS or R, a strong background in statistics, and a relevant degree such as in mathematics, statistics, or computer science. Experience with clinical trial data, CDISC standards (SDTM, ADaM), and regulatory submission processes, along with certifications like SAS Certified Professional, are highly valued. Exceptional problem-solving abilities, attention to detail, and effective communication enable you to manage complex datasets and collaborate with cross-functional teams. These combined skills ensure accurate data analysis, regulatory compliance, and successful delivery of biostatistical projects in the pharmaceutical or clinical research industry.
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Senior Statistical Programmer Analyst jobs near you
Infographic showing various Senior Statistical Programmer Analyst job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 5% Part Time, and 6% Contract. Highlights an 80% Physical, 9% Hybrid, and 11% Remote job distribution, with an average salary of $128,293 per year, or $61.7 per hour.

Senior Statistical Analyst

2T Consulting

Pelham, NY • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

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 and cross-functional teams to develop ADaM datasets, generate TLFs, support regulatory submissions, and ensure high-quality statistical programming deliverables for clinical studies.

Primary Responsibilities

*Collaborate with statisticians to develop and implement Statistical Programming Plans (SPPs) and Statistical Analysis Plans (SAPs).
*Program, validate, and maintain ADaM datasets, statistical analyses, and programming deliverables using SAS and R.
*Generate and validate Tables, Listings, and Figures (TLFs) for clinical study reports, safety reports, and regulatory submissions.
*Create and maintain programming documentation, including specifications, annotated code, validation plans, and programming guidelines.
*Perform quality control and validation of statistical programming outputs to ensure compliance with CDISC standards and regulatory requirements.
*Support ad hoc statistical analyses, exploratory data analyses, and data visualization requests.
*Develop and maintain reusable programming macros, utilities, and automation tools to improve efficiency and consistency.
*Provide programming support during regulatory submissions, audits, and inspections.
*Collaborate with study teams to resolve programming and data-related issues while ensuring timely project delivery.
*Identify project risks, escalate issues when necessary, and provide regular status updates.
*Mentor and train junior programmers and contribute to continuous process improvement initiatives.
*Stay current with industry best practices, regulatory guidelines, and advancements in statistical programming.

Required Skills & Qualifications

*Strong proficiency in SAS and R programming for clinical trial data analysis.
*Experience programming and validating ADaM datasets, TLFs, and statistical analyses.
*Advanced knowledge of CDISC standards, including ADaM and SDTM.
*Solid understanding of clinical trial processes, statistical methodologies, and regulatory requirements.
*Experience in therapeutic areas such as Oncology, Immunology, Neuroscience, or other clinical domains.
*Strong analytical, troubleshooting, and problem-solving skills.
*Excellent attention to detail with a strong focus on quality and compliance.
*Effective written and verbal communication skills.
*Ability to collaborate with statisticians, clinical study teams, and external stakeholders.
*Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

Preferred Qualifications

*Experience supporting global clinical trials and regulatory submissions.
*Knowledge of clinical data visualization and exploratory data analysis.
*Experience developing standardized SAS macros and programming utilities.
*Prior experience mentoring or leading statistical programming teams.
*Familiarity with FDA, EMA, and ICH regulatory guidelines for clinical data submissions.

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