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Statistical Programmer Analyst Jobs (NOW HIRING)

CON-Statistical Programmer

San Diego, CA ยท On-site

$75 - $100/hr

The Contract Statistical Programmer supports statistical analysis and reporting for clinical studies and related regulatory deliverables as an individual contributor on assigned projects. Primary ...

CON-Statistical Programmer

San Diego, CA ยท On-site

$75 - $100/hr

The Contract Statistical Programmer supports statistical analysis and reporting for clinical studies and related regulatory deliverables as an individual contributor on assigned projects. Primary ...

Contribute to and review of statistical analysis plans and analysis datasets specifications and ... Anticipate statistical programming resource needs and work with management to ensure adequate ...

The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.

Statistical Programmer II

Minneapolis, MN ยท On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.

Statistical Programmer II

Atlanta, GA ยท On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.

Statistical Programmer II

Austin, TX ยท On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.

The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.

The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.

The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.

The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.

Statistical Programmer II

Dallas, TX ยท On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.

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Statistical Programmer Analyst information

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$62K

$100.7K

$152.5K

How much do statistical programmer analyst jobs pay per year?

As of Jul 5, 2026, the average yearly pay for statistical programmer analyst in the United States is $100,711.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,000.00 and $126,500.00 per year, depending on experience, location, and employer.

What are Statistical Programmer Analysts?

Statistical Programmer Analysts are professionals who develop, test, and maintain statistical programs for analyzing data, typically in industries such as healthcare, pharmaceuticals, finance, and research. They work closely with statisticians and data managers to ensure data is accurately processed and reported, often using programming languages like SAS, R, or Python. Their responsibilities include creating analysis datasets, generating tables, listings, and figures, and ensuring compliance with regulatory requirements. Statistical Programmer Analysts play a key role in transforming raw data into meaningful insights that support decision-making and research outcomes.

How do Statistical Programmer Analysts typically collaborate with clinical research teams during a study?

Statistical Programmer Analysts work closely with clinical research teams, including biostatisticians, data managers, and clinical project managers, to ensure accurate analysis and reporting of clinical trial data. They are responsible for programming data sets, creating statistical tables, listings, and figures, and validating results to support regulatory submissions or publications. Effective communication and collaboration are essential, as they often attend regular team meetings to discuss requirements, troubleshoot data issues, and ensure timelines are met. This teamwork fosters a dynamic environment where analytical and technical expertise directly contribute to the success of clinical research projects.

What are the key skills and qualifications needed to thrive as a Statistical Programmer Analyst, and why are they important?

To thrive as a Statistical Programmer Analyst, you need strong skills in statistical analysis, programming (especially in SAS, R, or Python), and a relevant degree in statistics, mathematics, or a related field. Familiarity with clinical trial data standards (like CDISC), data management systems, and regulatory submission requirements is often required, along with certifications in SAS or similar tools. Attention to detail, analytical thinking, and effective collaboration are critical soft skills for this role. These skills and qualities are vital to ensure accurate data analysis, regulatory compliance, and successful team-based project delivery in data-driven environments.

What is the difference between Statistical Programmer Analyst vs Data Analyst?

AspectStatistical Programmer AnalystData Analyst
Required CredentialsBachelor's in Statistics, Computer Science, 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 statistical analysisVarious industries including finance, marketing, healthcare; focus on data interpretation and reporting
Employer & Industry UsageCommon in clinical trials, biotech, pharma companiesWidely used across multiple sectors including business, finance, and healthcare

The main difference is that a Statistical Programmer Analyst primarily focuses on programming and analyzing clinical or research data using statistical software, while a Data Analyst often handles broader data interpretation and reporting across various industries. Both roles require similar technical skills but differ in industry focus and specific responsibilities.

More about Statistical Programmer Analyst jobs
What cities are hiring for Statistical Programmer Analyst jobs? Cities with the most Statistical Programmer Analyst job openings:
What are the most commonly searched types of Statistical Programmer Analyst jobs? The most popular types of Statistical Programmer Analyst jobs are:
Who are the top companies hiring for Statistical Programmer Analyst jobs? The top employers for Statistical Programmer Analyst jobs are:
What states have the most Statistical Programmer Analyst jobs? States with the most job openings for Statistical Programmer Analyst jobs include:
What job categories do people searching Statistical Programmer Analyst jobs look for? The top searched job categories for Statistical Programmer Analyst jobs are:
Infographic showing various Statistical Programmer Analyst job openings in the United States as of June 2026, with employment types broken down into 33% Full Time, 39% Part Time, and 28% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $100,711 per year, or $48.4 per hour.
Senior Statistical Programmer

Senior Statistical Programmer

Katalyst HealthCares & Life Sciences

Los Angeles, CA โ€ข On-site

Other

Posted 2 days ago


Job description

Sr. Statistical Programmer

The Sr. Statistical Programmer supports the Biostatistics team in the generation and validation of analysis datasets and statistical outputs for clinical trials. This role is key to implementing programming standards and supporting the standardization of CDISC-compliant datasets (e.g., SDTM, ADaM) across clinical programs. Develop and validate SAS programs to generate analysis datasets, tables, listings, and figures (TLFs) that support clinical trial reporting, regulatory submissions, and publications. Implement and maintain standardized programming templates, macros, and tools to ensure consistency, efficiency, and compliance across clinical studies. Contribute to the creation and review of programming specifications for SDTM and ADaM like datasets based on CDISC standards and internal guidelines. Assist in programming support for data cleaning, interim analyses, medical review, and final study reports. Collaborate with statisticians, data managers, clinical team members, and external vendors to ensure timely and high-quality deliverables. Review Statistical Analysis Plans (SAP) with biostatisticians to anticipate any complications or complexities for programming activities. Perform quality control (QC) and validation of internally and externally developed datasets and outputs, adhering to company SOPs and programming best practices. Integrate data across multiple studies for pooled analyses, submission packages, or visual summaries to support regulatory filings or internal strategy. Document all programming activities clearly and thoroughly, supporting reproducibility and regulatory compliance in a validated programming environment. Use version control systems and structured documentation to support audit readiness and collaborative programming practices. Contribute to posters, presentations, or ad hoc analyses, including visual data summaries using SAS graphics or other data visualization tools. Other duties as required.

Bachelor's degree or higher in Statistics, Computer Science, Mathematics, Life Sciences, or a related discipline. 5+ years of experience in statistical programming within the pharmaceutical, biotechnology, or medical device industry. Candidate is a detail-oriented statistical programmer with a strong interest in clinical data analysis, regulatory processes (such as PMA or 510(k) submissions), and continual learning in a regulated environment. Understanding of clinical trial design, GxP principles, and FDA/EMA regulatory requirements, particularly for medical device submissions such as PMA and 510(k). Familiarity with CDISC standards (SDTM, ADaM); ability to implement standardized datasets in line with internal and industry guidelines. Strong attention to detail, problem-solving mindset, and ability to work independently or in a team environment. Effective communication skills and a collaborative approach to working with cross-functional teams.


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About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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