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Principal Statistical Programmer Jobs in Arizona

Three Point Solutions

Principal R&D Engineer

Tempe, AZ · On-site

$55 - $65/hr

Principal R&D Engineer Client: Medical Device Manufacturing Company Duration: 8.5 Months ... Analyze manufacturing data using statistical methods to drive process improvements and solve ...

NOAO

Principal AI Engineer

Tucson, AZ

Apply machine learning, statistical modeling, and AI techniques to large-scale scientific datasets ... Principal Engineer, AI Technical Lead, Architect, or equivalent senior technical leadership role.

NSF's NOIRLab

Principal AI Engineer

Tucson, AZ · On-site

$179K - $226K/yr

Apply machine learning, statistical modeling, and AI techniques to large-scale scientific datasets ... Principal Engineer, AI Technical Lead, Architect, or equivalent senior technical leadership role.

Teaching with Telescopes

Principal AI Engineer

Tucson, AZ · On-site

$179 - $226/hr

Apply machine learning, statistical modeling, and AI techniques to large-scale scientific datasets ... Principal Engineer, AI Technical Lead, Architect, or equivalent senior technical leadership role.

AURA

Principal AI Engineer

Tucson, AZ · On-site

$179K - $226K/yr

Apply machine learning, statistical modeling, and AI techniques to large-scale scientific datasets ... Principal Engineer, AI Technical Lead, Architect, or equivalent senior technical leadership role.

Rubin Obs

Principal AI Engineer

Tucson, AZ · On-site

$179 - $226/hr

Apply machine learning, statistical modeling, and AI techniques to large-scale scientific datasets ... Principal Engineer, AI Technical Lead, Architect, or equivalent senior technical leadership role.

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All JobsPrincipal Statistical Programmer JobsPrincipal Statistical Programmer Jobs in Arizona

Principal Statistical Programmer information

See Arizona salary details

$51

$78

$108

How much do principal statistical programmer jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for principal statistical programmer in Arizona is $78.80, according to ZipRecruiter salary data. Most workers in this role earn between $67.88 and $90.96 per hour, depending on experience, location, and employer.

What is a principal statistical programmer?

A Principal Statistical Programmer is a senior-level professional responsible for developing, validating, and maintaining statistical programs used in clinical trials and regulatory submissions. They ensure data accuracy, adherence to industry standards (such as CDISC), and compliance with regulatory requirements. They collaborate with statisticians, data managers, and clinical teams to analyze and report trial results. Additionally, they may mentor junior programmers and contribute to process improvements in statistical programming workflows.

What are the typical daily responsibilities of a principal statistical programmer in a clinical research setting?

As a Principal Statistical Programmer, your daily responsibilities often include developing, validating, and maintaining complex statistical programs to support clinical trial data analysis and regulatory submissions. You may lead programming teams, mentor junior staff, and act as a technical expert on study projects, collaborating closely with statisticians, data managers, and clinical teams. The role frequently involves reviewing statistical analysis plans (SAPs), generating data listings and summary tables, and ensuring adherence to industry standards such as CDISC. Effective communication and time management are key, as you’ll often work on multiple projects simultaneously, balancing deliverables and troubleshooting technical challenges. This position offers diverse, impactful work where your expertise significantly contributes to the integrity and success of clinical research programs.

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

To thrive as a Principal Statistical Programmer, you need advanced expertise in statistical programming (typically with SAS or R), a strong understanding of clinical trial data, and a degree in a relevant field such as statistics, mathematics, or computer science. Familiarity with CDISC standards (SDTM, ADaM), regulatory submission requirements, and project management tools is highly valued, and certifications like SAS Certified Advanced Programmer can be advantageous. Leadership, problem-solving, attention to detail, and excellent communication skills are important for managing complex projects and collaborating across multidisciplinary teams. These skills collectively ensure accuracy, regulatory compliance, and successful delivery of statistical programming support within clinical research environments.

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Principal Statistical Programmer jobs near you
Infographic showing various Principal Statistical Programmer job openings in Arizona as of August 2026, with employment types broken down into 88% Full Time, 9% Part Time, 2% Temporary, and 1% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $163,904 per year, or $78.8 per hour.

Principal R&D Engineer

Three Point Solutions, Inc.

Tempe, AZ • On-site

Full-time

Re-posted 8 days ago

Job description

Job Title: Principal R&D Engineer
Client: Medical Device Manufacturing Company
Duration: 8.5 Months (Possibility of Extension)
Location: Tempe, AZ 85281
Shift: 1st Shift
Description:
  • Lead the development, validation, and optimization of medical device manufacturing processes.
  • Design and execute process characterization, validation (IQ/OQ/PQ), DOE, and TMV activities.
  • Analyze manufacturing data using statistical methods to drive process improvements and solve complex engineering problems.
  • Collaborate with cross-functional teams to support product development, manufacturing readiness, and commercialization.
  • Conduct root cause investigations and implement corrective actions using DMAIC, 5 Whys, and Lean Six Sigma methodologies.
  • Ensure compliance with quality management systems, regulatory requirements, and validation standards.
  • Lead technical projects, mentor team members, and communicate project progress, risks, and solutions.
  • Support research, product development, and continuous improvement initiatives for medical devices.

Required Skills:
  • Process Development & Validation (DOE, IQ/OQ/PQ, TMV)
  • Statistical Analysis
  • Root Cause Analysis
  • Medical Device Manufacturing
  • Cross-Functional Project Leadership
  • Quality Management Systems (QMS)
  • Technical Problem Solving
  • Project Management
  • Risk Management
  • Technical Documentation

Preferred Skills:
  • HPLC, LCMS, FTIR, Mass Spectrometry
  • Lean Six Sigma / DFSS / DRM
  • Green Belt Certification
  • Technical Writing
  • Investigation & CAPA
  • Medical Device Regulatory Compliance

Education:
  • Advanced degree in Mechanical Engineering, Biomedical Engineering, Materials Science, Physics, Chemistry, Chemical Engineering, or a related engineering/science discipline.

Experience:
  • 7+ years of relevant R&D or manufacturing engineering experience, or
  • 5+ years of relevant experience with an advanced degree.
  • Experience in medical device process development, validation, and cross-functional project leadership is required.

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