Statistical Analyst
South Orange, NJ · On-site
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 ...
South Orange, NJ · On-site
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 ...
South Orange, NJ · On-site
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 ...
The Manager of Statistical Programming is a strategic role which guides a team of Statistical Programmers in the research and development of new pharmaceutical products. This role is directly ...
The Manager of Statistical Programming is a strategic role which guides a team of Statistical Programmers in the research and development of new pharmaceutical products. This role is directly ...
The Manager of Statistical Programming is a strategic role which guides a team of Statistical Programmers in the research and development of new pharmaceutical products. This role is directly ...
The Manager of Statistical Programming is a strategic role which guides a team of Statistical Programmers in the research and development of new pharmaceutical products. This role is directly ...
Head of Statistical Programming Location: South San Francisco, CA or Princeton, NJ - On-site 4 days per week (Mon to Thurs) Job Overview: The Senior Manager of Statistical Programming will be ...
Head of Statistical Programming Location: South San Francisco, CA or Princeton, NJ - On-site 4 days per week (Mon to Thurs) Job Overview: The Senior Manager of Statistical Programming will be ...
The Senior Director of Statistical Programming is responsible for the strategic direction, operational execution, people leadership, and quality of the Statistical Programming function at LB ...
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The Senior Director of Statistical Programming is responsible for the strategic direction, operational execution, people leadership, and quality of the Statistical Programming function at LB ...
New
The Senior Director of Statistical Programming is responsible for the strategic direction, operational execution, people leadership, and quality of the Statistical Programming function at LB ...
The Senior Director of Statistical Programming is responsible for the strategic direction, operational execution, people leadership, and quality of the Statistical Programming function at LB ...
The Senior Director of Statistical Programming is responsible for the strategic direction, operational execution, people leadership, and quality of the Statistical Programming function at LB ...
The Senior Director of Statistical Programming is responsible for the strategic direction, operational execution, people leadership, and quality of the Statistical Programming function at LB ...
Princeton, NJ · On-site
$75 - $80/hr
The Senior Statistical Programmer plays a critical role in supporting clinical development programs by providing expert statistical programming leadership across ongoing studies, regulatory ...
Princeton, NJ · On-site
$75 - $80/hr
The Senior Statistical Programmer plays a critical role in supporting clinical development programs by providing expert statistical programming leadership across ongoing studies, regulatory ...
Bridgewater, NJ · On-site +1
$170K - $205K/yr
Represent the company and the Statistical Programming department in business development and client relationship management initiatives. Provide leadership and oversight to the assigned client ...
Bridgewater, NJ · On-site +1
$170K - $205K/yr
Represent the company and the Statistical Programming department in business development and client relationship management initiatives. Provide leadership and oversight to the assigned client ...
The Statistical Programming community at Novartis comprises of approximately 350 (internal) statistical programmers and belongs to the Advanced Quantitative Sciences (AQS) organization which also ...
The Statistical Programming community at Novartis comprises of approximately 350 (internal) statistical programmers and belongs to the Advanced Quantitative Sciences (AQS) organization which also ...
Hoboken, NJ · On-site
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 ...
Hoboken, NJ · On-site
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 ...
Nutley, NJ · On-site
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 ...
Nutley, NJ · On-site
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 ...
Brooklyn, NY · On-site
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 ...
Brooklyn, NY · On-site
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 ...
Secaucus, NJ · On-site
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 ...
Secaucus, NJ · On-site
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 ...
Belleville, NJ · On-site
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 ...
Belleville, NJ · On-site
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 ...
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 ...
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 ...
Hillside, NJ · On-site
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 ...
Hillside, NJ · On-site
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 ...
$233K - $244K/yr
The Director of Statistical Programming is a pivotal, newly created role at LB Pharmaceuticals, reflecting our commitment to building a best-in-class internal Biometrics capability. This individual ...
$233K - $244K/yr
The Director of Statistical Programming is a pivotal, newly created role at LB Pharmaceuticals, reflecting our commitment to building a best-in-class internal Biometrics capability. This individual ...
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 ...
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 ...
Weehawken, NJ · On-site
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 ...
Weehawken, NJ · On-site
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 ...
| Aspect | Statistical Engineering | Data Scientist |
|---|---|---|
| Required credentials | Statistics, Data Analysis, Engineering | Statistics, Computer Science, Data Analysis |
| Work environment | Manufacturing, R&D, Engineering teams | Business, Tech, Research sectors |
| Employer usage | Optimizing processes, designing experiments | Building models, insights, predictive analytics |
Statistical Engineering focuses on applying statistical methods to improve engineering processes and product development, often within manufacturing or R&D settings. Data Scientists analyze large datasets to extract insights, build predictive models, and support business decisions. While both roles require strong statistical skills, Statistical Engineering emphasizes process optimization and experimental design, whereas Data Scientists focus on data-driven insights across diverse industries.
The top searched job categories for Statistical Engineering jobs in Basking Ridge, NJ are:
Cities near Basking Ridge, NJ with the most Statistical Engineering job openings:
Full-time
This job post has expired today. Applications are no longer accepted.
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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51 - 200 Employees
Edison, NJ, US