Senior Statistical Programmer Jobs in New Jersey
Senior Statistical Programmer jobs in New Jersey are consistently in demand, concentrated in the pharmaceutical, biotechnology, and clinical research sectors that define the state's economy from the Raritan Valley corridor through the northern suburbs. Most hiring centers on the Princeton, Parsippany, and Newark metro areas, where established employers like Johnson & Johnson, Merck, and Bristol Myers Squibb maintain major operations and regularly recruit at the senior level. The most sought-after specialties include SAS programming for clinical trials, CDISC standards implementation, and submission-ready regulatory output development. Find a role that fits below and apply directly.
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Provide support for clinical studies through dual expertise in statistical programming compliant with CDISC standards (SDTM/ADaM) and applied biostatistics. The role includes the production, validation, and review of CDISC deliverables, as well as the execution and support of statistical analyses.
Responsibilities
Participate in the design of clinical studies in collaboration with biostatisticians.
Contribute to the writing and review of Statistical Analysis Plans (SAPs).
Program and validate SDTM and ADaM datasets.
Produce, validate, and review SDTM/ADaM deliverables (annotated CRFs, specifications, datasets).
Ensure regulatory compliance using Pinnacle 21.
Participate in and validate regulatory submission deliverables (Define.xml, submission packages).
Perform Quality Control (QC) activities.
Produce and validate Tables, Listings, and Figures (TLFs).
Collaborate closely with clinical and regulatory teams.
Profile
Master's degree (MSc) or PhD in Biostatistics, Statistics, Mathematics, or a related field (e.g., ENSAI or equivalent).
Minimum of 6–8 years of experience in statistical programming for clinical trials, with strong expertise in CDISC standards (SDTM/ADaM).
Experience with regulatory submissions and CRO management is highly desirable.
Technical Skills
Proficiency in SAS (Base SAS, SAS Studio, SAS Viya).
Strong expertise in CDISC SDTM and ADaM standards.
Good knowledge of TLFs (Tables, Listings, and Figures) and regulatory requirements.
Experience using Pinnacle 21.
Solid understanding of clinical statistics.
Fluent English (written and spoken).
Behavioral Competencies
Curiosity
Continue exploring new horizons. Constantly ask "Why?" and, more importantly, "Why not?"
Courage
Take smart risks and support one another in continuously improving. Push boundaries, turn challenges into opportunities, and take ownership of our decisions, opinions, and actions.
Collaboration
Learn from one another. Grow and develop as a multicultural, international team working toward shared goals.
Credibility
Strive for excellence in everything we do. Transparency and expertise are the foundation of our relationships with patients, partners, and shareholders. Data and results are at the heart of our commitment.
Job Description
Provide support for clinical studies through dual expertise in statistical programming compliant with CDISC standards (SDTM/ADaM) and applied biostatistics. The role includes the production, validation, and review of CDISC deliverables, as well as the execution and support of statistical analyses.
Responsibilities
Participate in the design of clinical studies in collaboration with biostatisticians.
Contribute to the writing and review of Statistical Analysis Plans (SAPs).
Program and validate SDTM and ADaM datasets.
Produce, validate, and review SDTM/ADaM deliverables (annotated CRFs, specifications, datasets).
Ensure regulatory compliance using Pinnacle 21.
Participate in and validate regulatory submission deliverables (Define.xml, submission packages).
Perform Quality Control (QC) activities.
Produce and validate Tables, Listings, and Figures (TLFs).
Collaborate closely with clinical and regulatory teams.
Profile
Master's degree (MSc) or PhD in Biostatistics, Statistics, Mathematics, or a related field (e.g., ENSAI or equivalent).
Minimum of 6–8 years of experience in statistical programming for clinical trials, with strong expertise in CDISC standards (SDTM/ADaM).
Experience with regulatory submissions and CRO management is highly desirable.
Technical Skills
Proficiency in SAS (Base SAS, SAS Studio, SAS Viya).
Strong expertise in CDISC SDTM and ADaM standards.
Good knowledge of TLFs (Tables, Listings, and Figures) and regulatory requirements.
Experience using Pinnacle 21.
Solid understanding of clinical statistics.
Fluent English (written and spoken).
Behavioral Competencies
Curiosity
Continue exploring new horizons. Constantly ask "Why?" and, more importantly, "Why not?"
Courage
Take smart risks and support one another in continuously improving. Push boundaries, turn challenges into opportunities, and take ownership of our decisions, opinions, and actions.
Collaboration
Learn from one another. Grow and develop as a multicultural, international team working toward shared goals.
Credibility
Strive for excellence in everything we do. Transparency and expertise are the foundation of our relationships with patients, partners, and shareholders. Data and results are at the heart of our commitment.
See All 5 Senior Statistical Programmer Jobs in New Jersey
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Where New Jersey roles are concentrated, by current openings.
Senior Statistical Programmer Job Market in New Jersey
A snapshot from current New Jersey openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
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What New Jersey Employers Look For
The qualifications that appear most often in senior statistical programmer jobs across New Jersey.
- Bachelor's or advanced degree in statistics, biostatistics, mathematics, or a related quantitative field
- Proficiency in SAS programming with demonstrated experience in clinical trial data analysis
- Working knowledge of CDISC standards including SDTM and ADaM dataset development
- Five or more years of experience supporting regulatory submissions in a pharma or biotech environment
- Familiarity with FDA submission requirements and experience producing TLFs for clinical study reports
- Experience collaborating with biostatisticians, data managers, and regulatory teams in a regulated environment
Senior Statistical Programmer Jobs in New Jersey: Frequently Asked Questions
How do you become a senior statistical programmer in New Jersey?
Most senior statistical programmers in New Jersey come up through a degree in biostatistics, statistics, or a related quantitative field, followed by entry-level programming roles within pharma or CRO environments. New Jersey does not require a state-issued license for this role, but employers strongly favor candidates with SAS Base Programmer certification and demonstrated CDISC compliance experience. Given the concentration of clinical research employers along the Route 1 corridor, building experience with submission-ready datasets and regulatory output is the most direct path to senior-level roles in the state.
How much do senior statistical programmers make in New Jersey?
Senior statistical programmers in New Jersey earn a median of about $118,280 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $69,490 for the lowest 10% to over $180,790 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire senior statistical programmers in New Jersey?
Employers hiring senior statistical programmers in New Jersey right now include Everest Clinical Research, Regeneron, and DBV Technologies, based on current listings on Migrate Mate as of August 2026. New Jersey's dense concentration of pharmaceutical headquarters and contract research organizations makes it one of the most active states for this role nationwide.
Which New Jersey cities have the most senior statistical programmer jobs?
Bridgewater, New Jersey, and Warren have the most senior statistical programmer openings in New Jersey. Princeton and the surrounding Raritan Valley area anchor much of the demand thanks to the regional headquarters of major pharmaceutical and biotech companies, while Parsippany and areas closer to Newark reflect the broader northern New Jersey cluster of life sciences and CRO offices that draw consistent hiring volume.
Are there remote senior statistical programmer jobs in New Jersey?
Yes, and more than most fields. About 100% of senior statistical programmer openings tied to New Jersey are remote or hybrid as of August 2026, reflecting how much of the core work involves SAS programming, data review, and report generation that translates well to distributed teams. Roles tied to active clinical trials or requiring close collaboration with on-site biostatistics teams are more likely to require at least a hybrid schedule.
How can I get hired as a senior statistical programmer in New Jersey with little or no experience?
The most realistic entry path is joining a contract research organization or a mid-size pharma company in a junior or associate statistical programmer role, then building direct trial experience from within. New Jersey employers like ICON, Syneos Health, and Certara operate offices in the state and regularly bring on entry-level programmers to support study delivery teams. Earning a SAS Base Programmer certification before applying and familiarizing yourself with CDISC fundamentals substantially improves your competitiveness for these associate-level openings.
Where can I find and apply to senior statistical programmer jobs in New Jersey?
You can find and apply to senior statistical programmer jobs in New Jersey on Migrate Mate, which lists current New Jersey openings updated regularly. Search the available roles, find the ones that fit your background and preferred location, and apply directly to the employers posting them.
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