ZipRecruiter

Log In

1

Senior Statistical Programmer Analyst Jobs in Princeton Junction, NJ

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

Senior Statistical Programmer The Senior Statistical Programmer will provide comprehensive ... Collaborate with vendors to ensure accurate programming for analysis and regulatory submissions.

next page

Showing results 1-20

All JobsStatistical Programmer Analyst JobsSenior Statistical Programmer Analyst JobsSenior Statistical Programmer Analyst Jobs in Princeton Junction, NJ

Senior Statistical Programmer Analyst information

See Princeton Junction, NJ salary details

$86.8K

$135.1K

$176.3K

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

As of Sep 6, 2026, the average yearly pay for senior statistical programmer analyst in Princeton Junction, NJ is $135,057.00, according to ZipRecruiter salary data. Most workers in this role earn between $112,600.00 and $155,800.00 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.

What are popular job titles related to Senior Statistical Programmer Analyst jobs in Princeton Junction, NJ?

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

What cities near Princeton Junction, NJ are hiring for Senior Statistical Programmer Analyst jobs?

Cities near Princeton Junction, NJ with the most Senior Statistical Programmer Analyst job openings:

    Senior Statistical Programmer Analyst jobs near you
    Infographic showing various Senior Statistical Programmer Analyst job openings in Princeton Junction, NJ as of August 2026, with employment types broken down into 86% Full Time, 9% Part Time, and 5% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $135,057 per year, or $64.9 per hour.

    Sr. Statistical Programmer

    Solomon Page

    Princeton, NJ • On-site

    $75 - $80/hr

    Contractor

    Medical, Dental, Vision, Retirement

    Posted 12 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 .
    Opportunity Awaits.
    #LI-MB7

    Apply