ZipRecruiter

Log In

1

Senior Statistical Programmer Jobs in Newtown, CT

ASML USA

Senior Process Engineer - MRF

Wilton, CT · On-site

$107K - $139K/yr

Job Summary ASML Wilton is seeking a Senior Process Engineer to join the Wilton Factory Optics team ... CNC deterministic polishing statistical process control methods advanced CNC deterministic ...

New

ASML

Senior Process Engineer - MRF

Wilton, CT · On-site

$107K - $139K/yr

Job Summary ASML Wilton is seeking a Senior Process Engineer to join the Wilton Factory Optics team ... statistical and analytical methods • Ensure corrective actions are verified, embedded, and ...

WSP

Senior Geotechnical Engineer

Shelton, CT · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

WSP is currently initiating a search for a Senior Geotechnical Engineer for our Geotechnical and ... statistical analysis of rock and soil environmental data, and reporting. * Determine well-defined ...

BestEx Research

Execution Analyst

Stamford, CT · On-site

You will work closely with senior analysts and product specialists and grow with their support into ... Proven programming, statistics, and data analysis skills (e.g., Python, SQL, R) * Strong analytical ...

Bestex Research

Execution Analyst

Stamford, CT · On-site

You will work closely with senior analysts and product specialists and grow with their support into ... Proven programming, statistics, and data analysis skills (e.g., Python, SQL, R) * Strong analytical ...

ASML

Senior Process Engineer - Optical Fabrication

Wilton, CT · On-site

$107K - $139K/yr

Job Summary ASML Wilton is seeking a Senior Process Engineer to join the Optical Fabrication team ... statistical and analytical methods • Ensure corrective actions are verified, embedded, and ...

ASML

Senior Process Engineer - Optical Fabrication

Wilton, CT · On-site

$107K - $139K/yr

Job Summary ASML Wilton is seeking a Senior Process Engineer to join the Optical Fabrication team ... statistical and analytical methods • Ensure corrective actions are verified, embedded, and ...

Medtronic

Senior Process Engineer - North Haven, CT

North Haven, CT · On-site

$103K - $133K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

A Day in the Life The Senior Process Engineer is responsible for providing support for multiple ... Experience applying statistical methods and science-based decision making to design experiments and ...

New

Medtronic

Senior Process Engineer - North Haven, CT

North Haven, CT · On-site

$103K - $133K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

A Day in the Life The Senior Process Engineer is responsible for providing support for multiple ... Experience applying statistical methods and science-based decision making to design experiments and ...

New

Medtronic

Senior Process Engineer - North Haven, CT

North Haven, CT · On-site

$103K - $133K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

A Day in the Life The Senior Process Engineer is responsible for providing support for multiple ... Experience applying statistical methods and science-based decision making to design experiments and ...

New

Medtronic

Senior Process Engineer - North Haven, CT

North Haven, CT · On-site

$103K - $133K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

A Day in the Life The Senior Process Engineer is responsible for providing support for multiple ... Experience applying statistical methods and science-based decision making to design experiments and ...

New

next page

Showing results 1-20

All JobsStatistical Programmer JobsSenior Statistical Programmer JobsSenior Statistical Programmer Jobs in Newtown, CT

Senior Statistical Programmer information

See Newtown, CT salary details

$85K

$132.2K

$172.5K

How much do senior statistical programmer jobs pay per year?

As of Aug 17, 2026, the average yearly pay for senior statistical programmer in Newtown, CT is $132,155.00, according to ZipRecruiter salary data. Most workers in this role earn between $110,200.00 and $152,500.00 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 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 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 popular job titles related to Senior Statistical Programmer jobs in Newtown, CT?

For Senior Statistical Programmer jobs in Newtown, CT, the most frequently searched job titles are:

What cities near Newtown, CT are hiring for Senior Statistical Programmer jobs?

Cities near Newtown, CT with the most Senior Statistical Programmer job openings:

Senior Statistical Programmer jobs near you
Infographic showing various Senior Statistical Programmer job openings in Newtown, CT as of June 2026, with employment types broken down into 71% Full Time, and 29% Part Time. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $132,155 per year, or $63.5 per hour.

Manager, Clinical Programming (Remote)

Penfield Search Partners

Fairfield, CT • On-site, Remote

Full-time

Re-posted 2 days ago

Job description

Job Description Contact: Neisha Camacho/Terra Parsons - teamnt@penfieldsearch.com No 3rd party candidates Position Summary We are seeking an experienced Senior Clinical Programmer to support clinical development programs by delivering high-quality programming solutions for medical monitoring, data management, and statistical programming activities. The ideal candidate has strong expertise in CDISC standards, SDTM dataset development, and modern programming tools including SAS and R. This role partners closely with cross-functional teams to develop efficient, compliant, and scalable programming solutions that support ongoing clinical trials

Key Responsibilities Provide programming support for medical monitoring, data management, and statistical programming activities across clinical studies. Develop specifications for SDTM dataset creation in accordance with CDISC SDTM Implementation Guide (SDTM IG). Program, validate, and maintain CDISC-compliant SDTM datasets.

Create and maintain annotated CRFs (aCRFs) aligned with SDTM specifications. Generate outputs and listings to support medical monitoring, data review, statistical endpoint monitoring, and data management activities. Develop, enhance, and maintain SAS macros, R functions, and other reusable programming utilities.

Design, develop, test, and implement programming solutions to address complex business and study requirements. Ensure programming deliverables meet quality standards, timelines, and regulatory expectations. Collaborate effectively with cross-functional teams including Biostatistics, Data Management, Clinical Operations, and Medical Monitoring.

Manage multiple projects simultaneously while delivering high-quality work within established timelines. Qualifications Bachelor's degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related discipline (or equivalent experience). Experience programming in the pharmaceutical, biotechnology, or related regulated industry preferred.

Advanced programming proficiency in SAS, R, and SQL. Strong working knowledge of CDISC standards, including SDTM and annotated CRFs. Experience with JReview is highly preferred.

Experience with Shiny, Pharmaverse, and R Markdown is preferred. Familiarity with programming languages such as Python, VBA, or C++ is a plus. Excellent analytical, problem-solving, and communication skills.

Ability to work independently while collaborating effectively within cross-functional teams. Strong organizational skills with the ability to prioritize multiple assignments and meet deadlines. Preferred Experience Experience supporting medical review or clinical data review activities.

Experience developing reusable programming utilities and automation tools. Familiarity with regulatory submission standards and clinical trial data workflows. Experience working in a fast-paced clinical development environment.

Apply