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Principal Statistical Programmer Jobs in Arizona

Cytel

Principal Biostatistician FSP

Phoenix, AZ

Our Principal Biostatisticians provide statistical and development support and influence for the ... Oversight of internal programming activities and/or CRO contributions on assigned clinical trials ...

New

Cytel

Principal Biostatistician FSP

Phoenix, AZ · On-site

Our Principal Biostatisticians provide statistical and development support and influence for the ... Oversight of internal programming activities and/or CRO contributions on assigned clinical trials ...

New

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 ...

Medtronic

Principal Process Engineer

Tempe, AZ · On-site

Die Prep / Printed Circuit Board Assembly The Principal Process Engineer is responsible for ... Applies statistical methods and science-based decisions to design experiments and implement ...

Medtronic

Principal Process Engineer

Tempe, AZ · On-site

Die Prep / Printed Circuit Board Assembly The Principal Process Engineer is responsible for ... Applies statistical methods and science-based decisions to design experiments and implement ...

Medtronic

Principal Process Engineer

Tempe, AZ · On-site

Die Prep / Printed Circuit Board Assembly The Principal Process Engineer is responsible for ... Applies statistical methods and science-based decisions to design experiments and implement ...

MED Medtronic Inc

Principal Process Engineer

Tempe, AZ · On-site

$129 - $193/hr

Die Prep / Printed Circuit Board Assembly The Principal Process Engineer is responsible for ... Applies statistical methods and science‑based decisions to design experiments and implement ...

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.

NOAO

Principal AI Engineer

Tucson, AZ · On-site

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

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$78

$108

How much do principal statistical programmer jobs pay per hour?

As of Aug 30, 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.

What are popular job titles related to Principal Statistical Programmer jobs in Arizona?

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What job categories do people searching Principal Statistical Programmer jobs in Arizona look for?

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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, 10% Part Time, 1% Temporary, and 1% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $163,904 per year, or $78.8 per hour.

Principal Biostatistician FSP

Phoenix, AZ

Cytel
See more jobs at Cytelexternal

Full-time

Posted yesterday

New

Job description

Who Are You?

An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will lead one Phase I-IV clinical studies across your region. You are excited and enthusiastic, motivate your teams to do great work and collaborate easily with your clients. You never settle for what is, but always push clinical development forward to what it could be. You motivate others to do the same.

Sponsor-dedicated:

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Biostatistician you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.

Position Overview:

Our Principal Biostatisticians provide statistical and development support and influence for the associated client's trials providing expertise into processes, clinical development plans, concept sheets and protocols, as well as potentially providing oversight of work supported by other vendors. You will formulate integrated analytical approach to mine data sources, employ statistical methods, machine learning & deep learning algorithms to discover actionable insights and automate process for reducing effort and time for repeated use.

As a Principal Biostatistician, your responsibilities will include:

  • Lead statistical activities for assigned Clinical Trials (Phases 1 to 4) independently from protocol design to reporting of results.
  • Represent Statistics function on cross-functional trial (and possibly indication / project) teams and collaborate effectively with all cross-functional stakeholders.
  • Oversight of internal programming activities and/or CRO contributions on assigned clinical trials and other activities.
  • Contribute to or lead other activities from a statistical perspective as appropriate, including but not limited to Safety Reporting, ISS/ISE, addressing questions from Health Authorities, Publications.
  • Use SAS and/or R for purposes like QC of datasets and deliverables, inferential statistical analyses, modelling/simulation, exploratory analyses etc.
  • Contribute to and participate in other initiatives at Cytel or sponsor side as appropriate.
  • Oversight of more junior Statisticians as required.
  • Seeking an independent study level lead who
  • has a clear technical understanding of how to analyze clinical trial data properly (ICH E9 guideline)
  • experiences of representing biostats function to collaborate with stakeholders cross functionally
  • is equipped with strong communication skills
  • has a strong self-learning willingness to perform their own duties with minimum guidance.

Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:

  • Minimum of Bachelor's degree in statistics or a related discipline.
  • 9+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry.
  • Ability to work independently, demonstrate initiative and flexibility through effective and innovative leadership.
  • Attention to detail and quality focused, excellent interpersonal and communication skills, innovative, and collaborative behaviours
  • SAS programming skills for QCing critical outputs, Efficacy/Safety tables, and working closely with Programmers.
  • Knowledge of R programming (R Shiny/Python).

Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.

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