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Statistical Programmer Analyst Jobs in New Jersey

Solomon Page

Sr. Statistical Programmer

Princeton, NJ · On-site

$75 - $80/hr

The Senior Statistical Programmer plays a critical role in supporting clinical development programs ... Ad hoc analyses and reporting outputs * Ensure timely and high-quality delivery of programming ...

Actalent

Senior Statistical Programmer

Princeton, NJ · Hybrid

$70 - $80/hr

Collaborate with vendors to ensure accurate programming for analysis and regulatory submissions. * Participate in project teams, review protocols, statistical analysis plans, and clinical study ...

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

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

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 ...

2T Consulting

Senior Statistical Analyst

Belleville, 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

Secaucus, 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

Leonia, 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

Weehawken, 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 Analyst JobsStatistical Programmer Analyst Jobs in New Jersey

Statistical Programmer Analyst information

See New Jersey salary details

$62.9K

$102.2K

$154.8K

How much do statistical programmer analyst jobs pay per year?

As of Sep 5, 2026, the average yearly pay for statistical programmer analyst in New Jersey is $102,245.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,100.00 and $128,400.00 per year, depending on experience, location, and employer.

What is a statistical programmer analyst?

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.

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

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.

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 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.

What are the most commonly searched types of Statistical Programmer Analyst jobs in New Jersey?

The most popular types of Statistical Programmer Analyst jobs in New Jersey are:

What are popular job titles related to Statistical Programmer Analyst jobs in New Jersey?

For Statistical Programmer Analyst jobs in New Jersey, the most frequently searched job titles are:

What job categories do people searching Statistical Programmer Analyst jobs in New Jersey look for?

The top searched job categories for Statistical Programmer Analyst jobs in New Jersey are:

What are popular job titles related to Statistical Programmer Analyst jobs in NJ?

For Statistical Programmer Analyst jobs in NJ, the most frequently searched job titles are:

Statistical Programmer Analyst jobs near you
Infographic showing various Statistical Programmer Analyst job openings in New Jersey as of August 2026, with employment types broken down into 85% Full Time, 7% Part Time, 2% Temporary, and 6% Contract. Highlights an 79% Physical, 8% Hybrid, and 13% Remote job distribution, with an average salary of $102,245 per year, or $49.2 per hour.

Sr. Statistical Programmer

Solomon Page

Princeton, NJ • On-site

$75 - $80/hr

Contractor

Medical, Dental, Vision, Retirement

Posted 10 days ago

Job description

Our client is looking to fill the role of Senior Statistical Programmer.The Senior Statistical Programmer plays a critical role in supporting clinical development programs by providing expert statistical programming leadership across ongoing studies, regulatory submissions, and cross-functional initiatives. This position is responsible for the development, validation, and delivery of SDTM, ADaM, analysis datasets, tables, listings, and figures (TLFs), as well as patient profiles and ad hoc analyses. The successful candidate will serve as a primary programming representative on study teams, oversee external programming vendors, collaborate closely with Biostatistics, Data Management, Clinical Operations, and Regulatory Affairs, and contribute to the development and maintenance of global programming standards and processes. This role requires extensive experience supporting regulatory submissions, managing complex programming activities, and driving high-quality deliverables across multiple studies and development phases.
  • Hybrid in Princeton, NJ 2 days per week
  • $75-$80/hr
  • 1 year contract+

Responsibilities:
Study Programming and Deliverables
  • Independently manage and support multiple global clinical studies with minimal supervision.
  • Lead statistical programming activities for clinical trials, including the creation, validation, and maintenance of:
    • CDISC-compliant SDTM datasets
    • ADaM datasets
    • Tables, Listings, and Figures (TLFs)
    • Patient profiles
    • Ad hoc analyses and reporting outputs
  • Ensure timely and high-quality delivery of programming outputs for study milestones and regulatory submissions.

Vendor Oversight and Management
  • Provide oversight of external programming vendors responsible for SDTM, ADaM, TLFs, and related deliverables.
  • Review vendor-produced datasets, outputs, documentation, and validation packages to ensure quality, compliance, and consistency.
  • Coordinate vendor activities and facilitate communication to ensure adherence to study timelines and standards.

Cross-Functional Collaboration
  • Serve as the statistical programming representative on cross-functional study teams.
  • Collaborate with statisticians, data managers, clinical scientists, and regulatory teams throughout the study lifecycle.
  • Participate in protocol reviews, Statistical Analysis Plan (SAP) development, Clinical Study Report (CSR) reviews, and other key study activities.
  • Support Data Management activities, including data reconciliation and quality review processes.

Regulatory Submission Support
  • Support global regulatory submissions, including NDA, BLA, MAA, and supplemental submissions.
  • Develop and validate submission-ready datasets and analysis outputs.
  • Contribute to Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) programming activities.
  • Support responses to regulatory authority questions and information requests.
  • Ensure compliance with FDA, EMA, and other applicable regulatory requirements related to electronic submissions.

Process Improvement and Standards Development
  • Assist in the development, implementation, and maintenance of departmental programming standards, procedures, and best practices.
  • Support initiatives focused on process optimization, automation, innovation, and adoption of emerging technologies.
  • Collaborate with global colleagues, including teams in Japan, to ensure alignment of programming standards and operational processes.

Required Qualifications:
Education
  • Master's degree in Statistics, Computer Science, Data Science, Health Sciences, Biostatistics, or a related quantitative discipline required.

Experience
  • Minimum of 8 years of statistical programming experience within the pharmaceutical, biotechnology, or life sciences industry.
  • Extensive experience supporting clinical trials across multiple phases of development.
  • Demonstrated expertise in CDISC standards and regulatory submission requirements.
  • Proven experience supporting regulatory submissions, including ISS/ISE integration and CSR programming.
  • Experience responding to regulatory authority requests and queries.
  • Experience with safety reporting activities, including:
    • DSURs (Development Safety Update Reports)
    • Annual Safety Reports
    • Investigator Brochure updates
  • Experience with data integration across multiple studies for regulatory submissions is strongly preferred.
  • Experience with SAS Life Science Analytics Framework (SAS LSAF) is preferred.

Technical Skills
Required
  • Advanced proficiency in SAS (Base SAS, SAS/STAT, SAS/GRAPH, Reporting Procedures, Graphical Procedures, and SAS Macro programming).
  • Strong experience using SAS Version 9.2 or higher within a clinical research environment.
  • Expertise in CDISC standards, including:
    • CDASH
    • SDTM
    • ADaM
  • Strong understanding of electronic regulatory submission requirements and industry standards.
  • Knowledge of ICH-GCP guidelines and related regulatory requirements.
  • Advanced Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook.

Preferred
  • Experience programming in R and/or Python.
  • Familiarity with analytics automation, advanced visualization, and modern statistical programming technologies.

Key Competencies
  • Strong leadership and project management skills.
  • Ability to manage multiple priorities in a fast-paced global environment.
  • Excellent analytical and problem-solving abilities.
  • Strong communication and collaboration skills.
  • High attention to detail and commitment to quality.
  • Ability to work effectively with both internal stakeholders and external vendors.
  • Demonstrated commitment to process improvement and operational excellence.

If you meet the required qualifications and are interested in this role, please apply today.
Clinical Resource Network Distinction
CRN, a division of Solomon Page, offers a comprehensive benefits program for hourly employees. We pride ourselves on offering medical, dental, vision, 401(k), telehealth services, ESOP, and commuter benefits to our employees, including consultants - which sets us apart in the industries we serve.
About CRN
Founded in 2002, Clinical Resource Network (CRN), a division of Solomon Page, provides clinical research and talent solutions for pharmaceutical, biotech, and medical device companies. Focused on forming long-term relationships, services encompass contract staffing, project staffing, consultative services, and full-time placements. For more information, visit https://www.solomonpage.com/crn and connect with us on Facebook and LinkedIn .
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