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Associate Statistical Programmer Jobs in New Jersey

Kenvue

Principal Biostatistician

Short Hills, NJ · On-site

$127.08 - $179.40/hr

Associate Director Biostatistics Location: North America, United States, New Jersey, Summit Work ... statistical methods, and industry processes. * Proficiency in SAS or R programming. * Excellent ...

Kenvue

Principal Biostatistician

Chatham, NJ · On-site

$127.08 - $179.40/hr

Associate Director Biostatistics Location: North America, United States, New Jersey, Summit Work ... statistical methods, and industry processes. * Proficiency in SAS or R programming. * Excellent ...

Kenvue

Principal Biostatistician

New Providence, NJ · On-site

$127.08 - $179.40/hr

Associate Director Biostatistics Location: North America, United States, New Jersey, Summit Work ... statistical methods, and industry processes. * Proficiency in SAS or R programming. * Excellent ...

Kenvue

Principal Biostatistician

Springfield, NJ · On-site

$127.08 - $179.40/hr

Associate Director Biostatistics Location: North America, United States, New Jersey, Summit Work ... statistical methods, and industry processes. * Proficiency in SAS or R programming. * Excellent ...

Kenvue

Principal Biostatistician

Summit, NJ · On-site

$127.08 - $179.40/hr

Associate Director Biostatistics Location: North America, United States, New Jersey, Summit Work ... statistical methods, and industry processes. * Proficiency in SAS or R programming. * Excellent ...

Kenvue

Principal Biostatistician

Summit, NJ · On-site

$127.08 - $179.40/hr

Associate Director Biostatistics Location: North America, United States, New Jersey, Summit Work ... statistical methods, and industry processes. * Proficiency in SAS or R programming. * Excellent ...

Kenvue

Principal Biostatistician

Mountainside, NJ · On-site

$127.08 - $179.40/hr

Associate Director Biostatistics Location: North America, United States, New Jersey, Summit Work ... statistical methods, and industry processes. * Proficiency in SAS or R programming. * Excellent ...

Jj

Associate Director, MAA & RWE

Raritan, NJ · On-site

Learn more at Associate Director, Market Access Analytics and Real World Evidence (MAA & RWE ... Provide expert guidance on statistical methodologies and programming approaches to address key ...

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Showing results 21-40

All JobsAssociate Statistical Programmer JobsAssociate Statistical Programmer Jobs in New Jersey

Associate Statistical Programmer information

See New Jersey salary details

$85.8K

$149.5K

$252.8K

How much do associate statistical programmer jobs pay per year?

As of Sep 4, 2026, the average yearly pay for associate statistical programmer in New Jersey is $149,536.00, according to ZipRecruiter salary data. Most workers in this role earn between $126,900.00 and $162,400.00 per year, depending on experience, location, and employer.

What is an associate statistical programmer?

An Associate Statistical Programmer is an entry-level professional who assists in the programming and analysis of clinical trial data, primarily within the pharmaceutical or biotechnology industries. They use statistical software, such as SAS or R, to create, validate, and maintain datasets, tables, listings, and figures required for clinical study reports. Their work supports biostatisticians and clinical teams in ensuring data accuracy and regulatory compliance. This role is ideal for those with a background in statistics, mathematics, or computer science, looking to start a career in clinical data analysis.

How does an associate statistical programmer typically collaborate with biostatisticians and data managers in clinical research projects?

As an Associate Statistical Programmer, you will frequently collaborate with biostatisticians to understand statistical analysis plans and translate them into clear programming specifications. You’ll also work closely with data managers to ensure data integrity and resolve any data discrepancies before analysis. Effective communication and teamwork are essential, as you’ll often participate in project meetings, provide programming support, and help deliver high-quality datasets and reports under tight timelines. This collaborative environment is key to ensuring accurate and timely clinical trial results.

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

To thrive as an Associate Statistical Programmer, you need a solid background in statistics, programming (especially SAS or R), and familiarity with clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Proficiency with statistical software (such as SAS, R, or Python), CDISC standards, and data management tools is essential, and certifications in SAS programming can be advantageous. Attention to detail, strong problem-solving abilities, and effective communication skills help you collaborate with clinical teams and ensure data quality. These skills and qualities are vital for delivering accurate statistical analyses that support regulatory submissions and evidence-based decision-making in clinical research.

What is the difference between Associate Statistical Programmer vs Statistical Programmer?

AspectAssociate Statistical ProgrammerStatistical Programmer
Required CredentialsBachelor's degree in statistics, mathematics, or related field; some roles may require basic programming skillsBachelor's or master's degree; more experience in programming and statistical analysis
Work EnvironmentEntry-level, supporting senior programmers; often in clinical research or pharmaceutical companiesMore independent, handling complex analyses; similar industry settings
Employer & Industry UsageCommon in clinical trials, pharmaceutical, and biotech companiesUsed across similar industries, often as a step up from associate roles

The main difference between an Associate Statistical Programmer and a Statistical Programmer lies in experience and responsibility level. Associate roles are typically entry-level, focusing on supporting tasks under supervision, while Statistical Programmers handle more complex analyses independently. Both roles are vital in clinical research and biotech industries, with the associate position serving as a stepping stone to more advanced programming roles.

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

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

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

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

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

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

Associate Statistical Programmer jobs near you
Infographic showing various Associate Statistical Programmer job openings in New Jersey as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 25% Part Time, 2% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $149,536 per year, or $71.9 per hour.

Principal Biostatistician

Kenvue

Short Hills, NJ • On-site

$127.08 - $179.40/hr

Full-time

PTO

This job post has expired today. Applications are no longer accepted.

Kenvue rating

9.1

Company rating: 9.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

Kenvue is currently recruiting for a:

Principal Biostatistician

What we do

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated.  We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.

Role reports to:

Associate Director Biostatistics

Location:

North America, United States, New Jersey, Summit

Work Location:

Hybrid

What you will do

Principal Biostatistician manages the operations of the biostatistics functions of the department, including activities related to the design and analysis of clinical trials, data submission and ensure the project success, support the data interpretation and date reporting activities and publication strategy.

Key Responsibilities

  • Lead and manage biostatistics operations for clinical development programs, ensuring high-quality design, analysis, reporting, and interpretation of clinical trial data.
  • Serve as the Lead Statistical SME, applying appropriate statistical methodologies in alignment with established procedures and regulatory expectations.
  • Oversee statistical activities at the project level, including vendor oversight and ensuring compliance with statistical analysis and reporting standards.
  • Collaborate cross-functionally and with external partners to support project success, publication strategies, and manuscript development.
  • Provide statistical support for regulatory submissions and interactions with health authorities.
  • Support clinical investigators with statistical input and contribute to data interpretation, reporting activities, and scientific publications.

What We're Looking For

  • Graduate degree in Statistics or related quantitative field; typically 4+ years industry experience with a PhD or 6+ years with an MS.
  • Strong background in clinical development biostatistics, statistical methods, and industry processes.
  • Proficiency in SAS or R programming.
  • Excellent communication, collaboration, problem‑solving, and interpersonal skills; effective working in cross‑functional teams.
  • Advanced knowledge of working with CDISC and related FDA standards for the specification and creation of SDTM and ADaM datasets.
  • Strong ethical judgment and commitment to quality, compliance, and Credo-based decision-making.
  • Ability to contribute insights, challenge the status quo, and support innovative, data-driven solutions.
  • Demonstrated capability to identify risks, make effective decisions, manage priorities, and deliver results with speed and accountability.
  • Commitment to personal development and supporting team and talent growth; values diverse perspectives and fosters a trusting, collaborative environment.
  • Scientific curiosity and eagerness to grow expertise in statistical applications for clinical trials.

What’s in it for you

Annual base salary for new hires in this position ranges:

$127.075,00 - $179.400,00

This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.

  • Competitive Benefit Package*

  • Paid Company Holidays, Paid Vacation, Volunteer Time & More!

  • Learning & Development Opportunities

  • Kenvuer Impact Networks

  • This list could vary based on location/region

*Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

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