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Manager Statistical Programming Jobs in Rochester, NY

2T Consulting

Senior Statistical Analyst

York, NY · 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

Brighton, NY · 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

Brighton, NY · 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

York, NY · 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.

Kelly Services

Clinical Supply Manager

Rochester, NY

$47/hr

Internal customers to include Clinical Operations, Data Management, Statistics, Medical Affairs, Regulatory, Quality, Procurement, and Engineers. External customers/partners to include, Clinical ...

Pwc

CTIO - AI Engineer- Senior Manager

Rochester, NY

$91K - $321K/yr

In this role, you will engage in exploratory and descriptive analysis, statistical modeling, and ... Utilizing programming languages and machine learning libraries to optimize data workflows and ...

New

Pwc

Data Engineer - Manager

Rochester, NY

... Statistics - 5 years of experience What Sets You Apart - Certification in Cloud Platforms [e.g ... in programming languages such as Python, Java, or Scala - Familiarity with big data technologies ...

Puratos

Engineering Manager

Rochester, NY · On-site

On a project basis, this individual will play the role of Project Manager/Engineer himself/herself ... of statistical process improvement programs. Utilize Lean, Six Sigma and TPM methodologies to ...

Bausch & Lomb GmbH

Quality Engineer III

Rochester, NY · On-site

$95.20 - $128.80/hr

Nonconformance (NC) management and CAPA systems * Change control and validation activities ... Statistical sampling plans and data analysis * Design transfer activities in accordance with design ...

New

Pwc

CTIO AI Engineering Manager

Rochester, NY

$73K - $244K/yr

... Level Manager & Summary At PwC, our people in data and analytics engineering focus on leveraging ... You will work on developing predictive models, conducting statistical analysis, and creating data ...

Bausch + Lomb

Quality Engineer III

Rochester, NY · On-site

$95K - $128K/yr

Support decision-making through statistical tools Lead risk management activities aligned with iso ... The Senior Quality Engineer operates with a high level of independence and technical authority ...

General Motors

Manufacturing Quality Engineer

Rochester, NY · On-site

$80K - $109K/yr

Manufacturing Quality Engineer, able to work autonomously with occasional guidance from supervision ... Provide statistical analysis of manufacturing process data * Critical role in change management to ...

onsemi

Device Characterization Engineer

Hopewell, NY · On-site

$88K - $142K/yr

The successful candidate will leverage device physics knowledge, statistical analysis, and ... management and cross-functional teams. * Support reliability investigations and customer-facing ...

Pwc

US Tech - AI Engineering Manager

Rochester, NY

$73K - $244K/yr

You will work on developing predictive models, conducting statistical analysis, and creating data ... As a Manager you will combine engineering knowledge with people leadership to deliver resilient ...

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All JobsStatistical Programming JobsManager Statistical Programming JobsManager Statistical Programming Jobs in Rochester, NY

Manager Statistical Programming information

See Rochester, NY salary details

$83.9K

$146.2K

$247.2K

How much do manager statistical programming jobs pay per year?

As of Aug 20, 2026, the average yearly pay for manager statistical programming in Rochester, NY is $146,218.00, according to ZipRecruiter salary data. Most workers in this role earn between $124,100.00 and $158,800.00 per year, depending on experience, location, and employer.

What is a manager statistical programming?

A Manager Statistical Programming oversees a team of statistical programmers who support clinical trials and research by developing, validating, and maintaining statistical programs. They ensure compliance with regulatory requirements, manage project timelines, and collaborate with statisticians, data managers, and other stakeholders. This role requires strong programming skills in SAS or other statistical software, leadership abilities, and expertise in clinical data standards such as CDISC.

What are the typical daily responsibilities of a manager statistical programming?

As a Manager Statistical Programming, your daily responsibilities usually include overseeing a team of statistical programmers, coordinating the development and validation of statistical programs for clinical trial data analysis, and ensuring deliverables meet regulatory and company quality standards. You will often interact with biostatisticians, data managers, and clinical teams to align programming outputs with study goals. Additionally, you may review project timelines, allocate resources, mentor junior programmers, and contribute to process improvement initiatives. This multifaceted role requires balancing technical oversight with leadership and interdepartmental communication.

What are the key skills and qualifications needed to thrive in the manager statistical programming position, and why are they important?

To excel as a Manager Statistical Programming, you need a solid background in statistics, programming (such as SAS, R, or Python), and experience with clinical trial data management, often supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory guidelines (e.g., FDA, ICH), data standards such as CDISC, and certifications in relevant programming languages or clinical data processes are highly beneficial. Strong leadership, project management, and effective communication skills are essential for guiding teams and collaborating with cross-functional departments. These skills enable the manager to deliver high-quality statistical programming deliverables, ensure regulatory compliance, and drive team performance in a deadline-driven environment.

What are popular job titles related to Manager Statistical Programming jobs in Rochester, NY?

For Manager Statistical Programming jobs in Rochester, NY, the most frequently searched job titles are:

What job categories do people searching Manager Statistical Programming jobs in Rochester, NY look for?

The top searched job categories for Manager Statistical Programming jobs in Rochester, NY are:

What cities near Rochester, NY are hiring for Manager Statistical Programming jobs?

Cities near Rochester, NY with the most Manager Statistical Programming job openings:

Manager Statistical Programming jobs near you
Infographic showing various Manager Statistical Programming job openings in Rochester, NY as of August 2026, with employment types broken down into 100% Full Time. Highlights an 59% In-person, and 41% Remote job distribution, with an average salary of $146,218 per year, or $70.3 per hour.

Senior Statistical Analyst

2T Consulting

York, NY • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

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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