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Statistical Programmer Ii Jobs (NOW HIRING)

Eisai

Senior Manager, Statistical Programming

Nutley, NJ · On-site

$138K - $182K/yr

The Sr. Manager, Statistical Programming is responsible for SAS programming activities supporting ... Some experience having led projects pertaining to Phase I & II studies * Significant experience in ...

Eisai

Senior Manager, Statistical Programming

Nutley, NJ

$138K - $182K/yr

The Sr. Manager, Statistical Programming is responsible for SAS programming activities supporting ... Some experience having led projects pertaining to Phase I & II studies * Significant experience in ...

Amgen, Inc.

Biostatistical Programming Manager

Basic Qualifications: • Doctorate degree OR • Master's degree and 2 years of statistical programming experience OR • Bachelor's degree and 4 years of statistical programming experience OR • ...

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Statistical Programmer Ii information

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$84.5K

$147.3K

$249K

How much do statistical programmer ii jobs pay per year?

As of Aug 11, 2026, the average yearly pay for statistical programmer ii in the United States is $147,292.00, according to ZipRecruiter salary data. Most workers in this role earn between $125,000.00 and $160,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a statistical programmer ii?

A Statistical Programmer II typically requires strong programming skills in SAS or R, experience with clinical trial data, and a relevant degree in statistics, mathematics, or computer science. Familiarity with CDISC standards, data management systems, and regulatory submission requirements is often expected. Attention to detail, problem-solving abilities, and effective communication are vital soft skills for collaborating with cross-functional teams and ensuring data integrity. These competencies help deliver accurate analyses and support regulatory compliance in clinical research environments.

What are some common challenges faced by a statistical programmer ii when collaborating with clinical project teams?

As a Statistical Programmer II, one common challenge is aligning the programming deliverables with the evolving needs of clinical project teams, especially when study protocols or analysis plans change. Effective communication is essential to clarify requirements and timelines with statisticians, data managers, and clinical researchers. Additionally, ensuring data quality and consistency across multiple studies while adhering to regulatory standards can be demanding. Proactively addressing these challenges with strong collaboration and attention to detail helps ensure successful project outcomes.

What is a statistical programmer ii?

Statistical Programmer IIs are professionals who use specialized software to analyze and manage large datasets, typically in clinical research or pharmaceutical settings. They are responsible for programming and validating statistical analyses, generating tables, listings, and figures, and ensuring data accuracy for regulatory submissions. This role requires proficiency in programming languages such as SAS or R, strong analytical skills, and a good understanding of clinical trial processes. Statistical Programmer IIs often work as part of a team, collaborating with statisticians and data managers to deliver high-quality data outputs.

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

AspectStatistical Programmer IiData Analyst
Required CredentialsBachelor's in Statistics, Computer Science, or related field; programming skills in SAS, R, or PythonBachelor's in Statistics, Data Science, or related field; proficiency in Excel, SQL, and visualization tools
Work EnvironmentPharmaceutical or clinical research settings, working with clinical trial dataBusiness, healthcare, or marketing sectors analyzing large datasets
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsCorporations, healthcare providers, market research firms

While both roles involve data analysis, Statistical Programmer Ii primarily focuses on programming and preparing clinical trial data, whereas Data Analysts interpret data to inform business decisions. The roles share similar educational backgrounds and technical skills but differ in industry focus and daily tasks.

More about Statistical Programmer Ii jobs
What cities are hiring for Statistical Programmer Ii jobs? Cities with the most Statistical Programmer Ii job openings:
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What job categories do people searching Statistical Programmer Ii jobs look for? The top searched job categories for Statistical Programmer Ii jobs are:
Statistical Programmer Ii jobs near you
Infographic showing various Statistical Programmer Ii job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, and 16% Contract. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $147,292 per year, or $70.8 per hour.

Junior Statistical Programmer

Oasis Technology Inc.

East Brunswick, NJ • On-site, Remote

Contractor

Re-posted 17 days ago

Job description

Company Description
Job Description
  • Minimum 2-3 years of experience defining SAS analysis requirements and performing SAS programming
  • BASE SAS cert
  • Expert knowledge of base SAS and SAS Macros for SAS software development
  • Design, development and unit-testing od SAS program code, functions and scripts to efficiently extract, merge and manipulate data
  • Expert Knowledge of lookup tables for SAS for SAS software development
  • Expert knowledge in proposing and implementing improvements/efficiencies for SAS software development to create repeatable business processes for use by others
  • Excellent oral and written communication skills in English
  • Experience clarifying business and technical requirements with data requestors
  • Provides technical and analytic input to peer review team

Qualifications
Education:
  • BA/BS or equivalent experience in mathematics, statistics computer science, life sciences or related field.

Additional skill set:
  • Expert knowledge of/experience with SAS software.
  • Good understanding of global clinical trials practices, procedures, methodologies.
  • Good understanding of regulatory requirements relevant to SR (e.g. GCP, ICH)
  • Experience in providing recommendations for maintenance or development of SR global policies, procedures and clinical data presentation standards.
  • Intermediate knowledge of office tools.
  • Experience in a pharmacetical company is must.

Additional Information
Visa Status
  • Only US Citizens, Green Card, EAD and OPT holders.
  • No H1B Holders and Third-Parties.
  • No Corp-Corp

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