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Senior Statistical Programmer Jobs in Wayne, NJ (NOW HIRING)

Eikon Therapeutics

Senior Manager, Biostatistics

Jersey City, NJ · On-site

$170K - $204K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Position We are seeking a skilled and highly motivated Senior Manager, Biostatistics to join our ... Their proficiency in statistical programming languages, understanding of regulatory guidelines, and ...

New

Eikon Therapeutics

Senior Manager, Biostatistics

Jersey City, NJ · On-site

$170K - $204K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Position We are seeking a skilled and highly motivated Senior Manager, Biostatistics to join our ... Their proficiency in statistical programming languages, understanding of regulatory guidelines, and ...

New

Capital One

Sr. Business Analyst - US Card

New York, NY · On-site

$101K - $130K/yr

Sr. Business Analyst - US Card Summary: As a Senior Business Analyst at Capital One, you will apply ... Statistics, Engineering * 1+ years of experience in Statistical model building * 1+ years of ...

Ramp

Senior Applied Scientist, Credit Risk

New York, NY · On-site

$165K - $228K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

About the Role We're looking for a Senior Applied Scientist to help drive the future of credit ... Bachelor's degree or above in Math, Economics, Bioinformatics, Statistics, Engineering, Computer ...

Altimmune

Director, Biostatistics

Morristown, NJ · On-site

Reporting to the Senior Director, Biostatistics, this individual will provide statistical ... Responsible for the overall quality of statistical design, programming, analysis, and data ...

Altimmune

Director, Biostatistics

Morristown, NJ · On-site

Reporting to the Senior Director, Biostatistics, this individual will provide statistical ... Responsible for the overall quality of statistical design, programming, analysis, and data ...

Altimmune

Director, Biostatistics

Morristown, NJ · On-site +1

Reporting to the Senior Director, Biostatistics, this individual will provide statistical ... Responsible for the overall quality of statistical design, programming, analysis, and data ...

ICF

Senior Climate Analytics Specialist

New York, NY · On-site

$95K - $117K/yr

ICF is seeking a Senior Climate Analytics Specialist with strong scientific programming and cloud ... Design, train, and rigorously validate machine learning and statistical models in data-limited and ...

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All JobsStatistical Programmer JobsSenior Statistical Programmer JobsSenior Statistical Programmer Jobs in Wayne, NJ

Senior Statistical Programmer information

See Wayne, NJ salary details

$81.8K

$127.2K

$166.1K

How much do senior statistical programmer jobs pay per year?

As of Aug 13, 2026, the average yearly pay for senior statistical programmer in Wayne, NJ is $127,238.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,100.00 and $146,800.00 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 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 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 popular job titles related to Senior Statistical Programmer jobs in Wayne, NJ?

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

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

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

Senior Statistical Programmer jobs near you
Infographic showing various Senior Statistical Programmer job openings in Wayne, NJ as of June 2026, with employment types broken down into 97% Full Time, 1% Part Time, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $127,238 per year, or $61.2 per hour.

Senior Principal Statistician, Biometrics

Ferring Pharmaceuticals

Parsippany, NJ • On-site

$191K - $225K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 days ago

Job description

Job Description:
As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our independence helps us cultivate an entrepreneurial spirit and long-term perspective that enables us to achieve growth and scale, while remaining agile and true to our 'people first' philosophy. Built on a 70-year plus commitment to science and research, Ferring is relentless in its pursuit of science that drives powerful discoveries and therapies to help people build families, stay healthy, and stand up to the world's oldest enemy: disease.
As a Senior Principal Statistician, Biometrics you will be part of clinical development teams, contributing to the design, execution, analysis, and reporting of development programs. You will support both traditional clinical trial activities and broader evidence generation efforts, integrating clinical and real-world data to inform development and regulatory decision-making.
With Ferring, you will be joining a recognized leader, identified as one of "The World's Most Innovative Companies" by Fast Company, and honored by Fortune with inclusion on its "Change the World List," for addressing society's unmet needs. Ferring US is also Great Places to Work® Certified, distinguishing it as one of the best companies to work for in the country.
Responsibilities:
Evidence generation and real-world evidence (RWE)
  • Supporting the design, conduct, analysis and reporting of RWE studies
  • Contribute to integrated evidence generation strategies combining clinical trial and real-world data
  • Supporting use of RWE in regulatory submissions, health technology assessment (HTA), and lifecycle planning

Clinical development and statistical contribution
  • Providing statistical input to clinical development plans and target product profiles
  • Authoring statistical analysis plans and contributing to study design
  • Supporting analysis and interpretation of clinical trial data
  • Contributing to clinical study reports and regulatory submissions

Assessment of business development opportunities
  • Critically review and evaluate clinical trial data to assess efficacy, safety, and asset value, including opportunities for life cycle management such as label expansion, new indications, and geographic growth.
  • Conduct gap analyses to identify missing data or limitations that may affect regulatory approval or market success and support the design of additional studies or registries to address these needs.
  • Provide statistical input and perform independent analyses of key endpoints, subgroups, and sensitivity results to validate asset potential and strengthen evidence generation strategies by integrating clinical trial and real-world data.
  • Contribute to due diligence reports, advise on statistical rigor, and evaluate the asset's readiness for regulatory submission, including review of analysis plans and submission documentation to inform business and scientific decisions.

Requirements:
  • Bachelor's degree required, Master's degree or PhD in Statistics, Biostatistics, or a related quantitative field preferred
  • 5+ years of experience working in the pharmaceutical industry•
  • Proficiency in statistical programming languages (e.g., R, SAS)•
  • Experience working with registry/claims data, including assessing the suitability and quality of such data sources in accordance with FDA guidance, and applying methodologies for analyzing observational data, e.g. constructing synthetic/external control arms, implementing the target trial emulation framework, or applying causal inference methods.•
  • Strong analytical thinking and ability to translate complex data into clear insights•
  • Effective communication skills, collaborative mindset and the ability to work in a dynamic environment

Ferring + you
At Ferring, we offer competitive total compensation along with an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work. From working hours that respect your lifestyle, a culture that is welcoming and equitable, and the chance to work with the industry's most impressive people, these are just some of the ways we live our "People First" philosophy.
Our Compensation and Benefits
At Ferring, base salary is one part of our competitive total compensation and benefits package and is determined using a salary range. The base salary range for this role is $191,000 to $225,000, which is the reasonable estimate of the base compensation for this role. The actual amount paid may differ based on non-discriminatory factors such as experience, knowledge, skills, abilities, education and primary work location. Additional compensation for this role will be provided based on competitive annual incentive compensation targets in the form of an annual bonus - payouts are based on individual and company performance.
Benefits for this role include comprehensive healthcare (medical, dental, and vision) with a premium differential, inverse to base salary, to be paid by employees, a 401k plan and company match, short and long-term disability coverage, basic life insurance, wellness benefits, reimbursement for certain tuition expenses, sick time of 1 hour per 30 hours worked, vacation time for full time employees to accrue up to 120 hours in the first four (4) years of employment, and 160 hours in the fifth (5th) year of employment as well as 15 paid holidays per year. We are proud to offer paid parental leave subject to a minimum period of employment at Ferring.
Ferring is an equal opportunity employer. All aspects of employment will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local laws.
Join our team and your voice will be heard, and your contributions will be valued. If you love to come up with new ways to make a positive difference and see them through, you will fit right in.
We are proud to be an Affirmative Action/Equal Opportunity Employer (including Disability/Protected Veterans). We maintain a drug-free workplace.
Location:
Parsippany, New Jersey

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