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Director Statistical Programming Jobs in Queens, NY

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 ...

The NPD Group, Inc.

Data Scientist

Port Washington, NY · On-site

This position will interact frequently with senior leadership teams and will direct and manage the ... statistical programming using SAS, R, and other languages * Familiarity with Agile methodology

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

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 ...

The NPD Group, Inc.

Data Scientist

Port Washington, NY · On-site

This position will interact frequently with senior leadership teams and will direct and manage the ... statistical programming using SAS, R, and other languages * Familiarity with Agile methodology

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

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 ...

CREW Carbon

Head of Technical Solutions

Manhattan, NY · On-site

$150 - $200/hr

... utility directors, chief engineers, operations leads - particularly trust-based, multi-year ... data.and experience with statistical programming and modeling (e.g., Python, R, MatLab)

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All JobsStatistical Programming JobsDirector Statistical Programming JobsDirector Statistical Programming Jobs in Queens, NY

Director Statistical Programming information

See Queens, NY salary details

$160.2K

$292.3K

$359K

How much do director statistical programming jobs pay per year?

As of Aug 22, 2026, the average yearly pay for director statistical programming in Queens, NY is $292,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $271,800.00 and $336,500.00 per year, depending on experience, location, and employer.

What is a director statistical programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

What does a director statistical programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.

What are the key skills and qualifications needed to thrive as a director statistical programming?

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

How does a director statistical programming typically collaborate with cross-functional teams in a pharmaceutical or biotech company?

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.
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Director Statistical Programming jobs near you

Principal Biostatistician

Kenvue

Chatham, 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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