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Senior Statistical Programmer Jobs in Somerville, 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 by providing expert statistical programming leadership across ongoing studies, regulatory ...

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Senior Statistical Programmer information

See Somerville, NJ salary details

$84.5K

$131.4K

$171.5K

How much do senior statistical programmer jobs pay per year?

As of Aug 31, 2026, the average yearly pay for senior statistical programmer in Somerville, NJ is $131,389.00, according to ZipRecruiter salary data. Most workers in this role earn between $109,600.00 and $151,600.00 per year, depending on experience, location, and employer.

What is a senior statistical programmer?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

What are the typical responsibilities and team dynamics for a senior statistical programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.

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

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

What are popular job titles related to Senior Statistical Programmer jobs in Somerville, NJ?

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

What cities near Somerville, NJ are hiring for Senior Statistical Programmer jobs?

Cities near Somerville, NJ with the most Senior Statistical Programmer job openings:

Senior Statistical Programmer jobs near you
Infographic showing various Senior Statistical Programmer job openings in Somerville, NJ as of August 2026, with employment types broken down into 1% Internship, 78% Full Time, 19% Part Time, and 2% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $131,389 per year, or $63.2 per hour.

Sr. Statistical Programmer

Solomon Page

Princeton, NJ • On-site

$75 - $80/hr

Contractor

Medical, Dental, Vision, Retirement

Posted 6 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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