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Senior Manager Statistical Programming Jobs in New Jersey

2T Consulting

Senior Statistical Analyst

Dumont, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

2T Consulting

Senior Statistical Analyst

Bogota, NJ

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

2T Consulting

Senior Statistical Analyst

Glen Ridge, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

2T Consulting

Senior Statistical Analyst

Wallington, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

2T Consulting

Senior Statistical Analyst

Oradell, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

2T Consulting

Senior Statistical Analyst

Moonachie, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

2T Consulting

Senior Statistical Analyst

Harrison, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

2T Consulting

Senior Statistical Analyst

Edgewater, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

2T Consulting

Senior Statistical Analyst

Tenafly, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

2T Consulting

Senior Statistical Analyst

Kearny, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

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 ... Study Programming and Deliverables * Independently manage and support multiple global clinical ...

2T Consulting

Senior Statistical Analyst

Montclair, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

2T Consulting

Senior Statistical Analyst

Bloomfield, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

2T Consulting

Senior Statistical Analyst

Closter, NJ · On-site

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC ... Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

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Senior Manager Statistical Programming information

How does a senior manager statistical programming typically collaborate with cross-functional teams in clinical research projects?

A Senior Manager Statistical Programming plays a pivotal role in coordinating with biostatisticians, clinical data managers, and medical writers to ensure seamless data flow and analysis throughout clinical trials. They oversee programming teams to deliver statistical outputs, such as tables, listings, and figures, while maintaining compliance with regulatory standards. Regular meetings and clear communication are essential, as the Senior Manager must interpret project requirements and translate them into actionable programming tasks, ensuring timelines and quality standards are met. This collaborative environment fosters continuous learning and problem-solving, as cross-functional input is vital for addressing complex data challenges.

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

To thrive as a Senior Manager Statistical Programming, you need expertise in biostatistics, programming languages like SAS or R, and experience with clinical trial data, typically supported by an advanced degree in a quantitative field. Familiarity with regulatory requirements (e.g., CDISC standards), clinical data management systems, and project management tools is essential. Strong leadership, communication, and problem-solving skills help you lead teams and liaise with cross-functional stakeholders. These skills ensure accurate, compliant data analyses and effective team management for successful clinical trial outcomes.

What is the difference between Senior Manager Statistical Programming vs Statistical Programmer?

AspectSenior Manager Statistical ProgrammingStatistical Programmer
CredentialsBachelor's/Master's in Biostatistics, Computer Science, or related field; often with management experienceBachelor's or Master's in Biostatistics, Statistics, or related field
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPerforms data analysis, programming, and validation tasks under supervision
Employer & Industry UsagePharmaceutical, biotech companies, CROs, clinical researchPharmaceutical, biotech, clinical research organizations

The main difference is that Senior Manager Statistical Programming oversees teams and manages projects, while Statistical Programmers focus on executing data analysis and programming tasks. The senior role involves leadership responsibilities, whereas the programmer role is more technical and task-oriented.

What are popular job titles related to Senior Manager Statistical Programming jobs in New Jersey?

For Senior Manager Statistical Programming jobs in New Jersey, the most frequently searched job titles are:

What job categories do people searching Senior Manager Statistical Programming jobs in New Jersey look for?

The top searched job categories for Senior Manager Statistical Programming jobs in New Jersey are:

What cities in New Jersey are hiring for Senior Manager Statistical Programming jobs?

Cities in New Jersey with the most Senior Manager Statistical Programming job openings:

Senior Manager Statistical Programming jobs near you
Infographic showing various Senior Manager Statistical Programming job openings in New Jersey as of August 2026, with employment types broken down into 83% Full Time, 15% Part Time, and 2% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution.

Senior Statistical Analyst

2T Consulting

Saddle Brook, NJ • On-site

Full-time

Posted 21 days ago

Job description

We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians and cross-functional teams to develop ADaM datasets, generate TLFs, support regulatory submissions, and ensure high-quality statistical programming deliverables for clinical studies.

Primary Responsibilities

*Collaborate with statisticians to develop and implement Statistical Programming Plans (SPPs) and Statistical Analysis Plans (SAPs).
*Program, validate, and maintain ADaM datasets, statistical analyses, and programming deliverables using SAS and R.
*Generate and validate Tables, Listings, and Figures (TLFs) for clinical study reports, safety reports, and regulatory submissions.
*Create and maintain programming documentation, including specifications, annotated code, validation plans, and programming guidelines.
*Perform quality control and validation of statistical programming outputs to ensure compliance with CDISC standards and regulatory requirements.
*Support ad hoc statistical analyses, exploratory data analyses, and data visualization requests.
*Develop and maintain reusable programming macros, utilities, and automation tools to improve efficiency and consistency.
*Provide programming support during regulatory submissions, audits, and inspections.
*Collaborate with study teams to resolve programming and data-related issues while ensuring timely project delivery.
*Identify project risks, escalate issues when necessary, and provide regular status updates.
*Mentor and train junior programmers and contribute to continuous process improvement initiatives.
*Stay current with industry best practices, regulatory guidelines, and advancements in statistical programming.

Required Skills & Qualifications

*Strong proficiency in SAS and R programming for clinical trial data analysis.
*Experience programming and validating ADaM datasets, TLFs, and statistical analyses.
*Advanced knowledge of CDISC standards, including ADaM and SDTM.
*Solid understanding of clinical trial processes, statistical methodologies, and regulatory requirements.
*Experience in therapeutic areas such as Oncology, Immunology, Neuroscience, or other clinical domains.
*Strong analytical, troubleshooting, and problem-solving skills.
*Excellent attention to detail with a strong focus on quality and compliance.
*Effective written and verbal communication skills.
*Ability to collaborate with statisticians, clinical study teams, and external stakeholders.
*Proven ability to manage multiple priorities and meet project deadlines in a fast-paced environment.

Preferred Qualifications

*Experience supporting global clinical trials and regulatory submissions.
*Knowledge of clinical data visualization and exploratory data analysis.
*Experience developing standardized SAS macros and programming utilities.
*Prior experience mentoring or leading statistical programming teams.
*Familiarity with FDA, EMA, and ICH regulatory guidelines for clinical data submissions.

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