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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 standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...

2T Consulting

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 ...

2T Consulting

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 ...

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 standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...

2T Consulting

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 ...

2T Consulting

Senior Statistical Analyst

Bronx, 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 ...

2T Consulting

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 ...

2T Consulting

Senior Statistical Analyst

Lyndhurst, 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 ...

2T Consulting

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 ...

2T Consulting

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 ...

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How much do senior statistical analyst jobs pay per year?

As of Aug 23, 2026, the average yearly pay for senior statistical analyst in the United States is $99,008.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,000.00 and $107,000.00 per year, depending on experience, location, and employer.

What is a senior statistical analyst?

Senior Statistical Analysts are experienced professionals who use advanced statistical methods to collect, analyze, and interpret complex data sets. They often design experiments, develop predictive models, and provide data-driven insights to support business decision-making. In addition to technical expertise, they may oversee junior analysts, collaborate with other departments, and present findings to stakeholders. Their work helps organizations understand trends, measure performance, and identify opportunities or risks.

How does a senior statistical analyst typically collaborate with cross-functional teams on large projects?

Senior Statistical Analysts often work closely with professionals from departments such as data engineering, product management, and business analytics. They translate complex statistical findings into actionable insights, ensuring that technical results are accessible to non-technical stakeholders. Collaboration may involve regular meetings, joint project planning sessions, and iterative feedback loops to refine analyses based on shifting business priorities. This collaborative environment not only enhances project outcomes but also provides opportunities for professional growth through exposure to diverse perspectives and expertise.

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

To thrive as a Senior Statistical Analyst, you need advanced knowledge of statistical theory, data analysis, and a relevant degree in statistics, mathematics, or a related field. Expertise with statistical software such as SAS, R, Python, and experience with data visualization tools are commonly required, along with certifications like SAS Certified Advanced Analytics Professional. Strong problem-solving abilities, attention to detail, and effective communication skills help you translate complex data into actionable insights. These skills ensure accurate analysis, informed decision-making, and clear communication of findings to stakeholders.
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Senior Statistical Analyst jobs near you
Infographic showing various Senior Statistical Analyst job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 5% Part Time, and 6% Contract. Highlights an 80% Physical, 9% Hybrid, and 11% Remote job distribution, with an average salary of $99,008 per year, or $47.6 per hour.

Senior Statistical Analyst

2T Consulting

Edgewater, NJ • On-site

Full-time

Posted 15 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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