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R Statistical Programmer Jobs in California (NOW HIRING)

Apple

NAND Q&R Engineer

Cupertino, CA · On-site

As an Apple NAND Q&R Engineer, you will shape the future of Apple's mass storage architecture by ... You'll integrate statistical insight with hardware quality and reliability data to optimize flash ...

Apple

NAND Q&R Engineer

Cupertino, CA · On-site

As an Apple NAND Q&R Engineer, you will shape the future of Apple's mass storage architecture by ... You'll integrate statistical insight with hardware quality and reliability data to optimize flash ...

Apple

NAND Q&R Engineer

Cupertino, CA

$147K - $272K/yr

Description As an Apple NAND Q&R Engineer, you will shape the future of Apple's mass storage ... You'll integrate statistical insight with hardware quality and reliability data to optimize flash ...

Apple

NAND Q&R Engineer

Cupertino, CA

$181K - $318K/yr

Description As an Apple NAND Q&R Engineer, you will shape the future of Apple's mass storage ... You'll integrate statistical insight with hardware quality and reliability data to optimize flash ...

Jazz Pharmaceutical

Sr Principal Statistician

Palo Alto, CA

$102K - $125K/yr

Experience in using SAS and R; knowledge of other statistical applications and programming languages a plus. * Knowledge of applicable regulatory requirements and guidelines, e.g., ICH Guidelines and ...

Jazz Pharmaceutical

Sr Principal Statistician

Palo Alto, CA · On-site +1

$102K - $125K/yr

Experience in using SAS and R; knowledge of other statistical applications and programming languages a plus. * Knowledge of applicable regulatory requirements and guidelines, e.g., ICH Guidelines and ...

Jazz Pharmaceuticals

Sr Principal Statistician

Palo Alto, CA

$102K - $125K/yr

Experience in using SAS and R; knowledge of other statistical applications and programming languages a plus. * Knowledge of applicable regulatory requirements and guidelines, e.g., ICH Guidelines and ...

Grainger Businesses

$78K - $83K/yr

... R (Statistical programing), SAP, SQL solutions. ▪ Negotiation skills and highly abstract and holistic thinking. ▪ Understanding of the competitive market and customer needs. ▪ Proven track ...

KLA

Staff Statistician

Milpitas, CA · On-site

... user of statistical software (e.g., JMP, Minitab, SPSS, R, or SAS). Some scripting and programming experience is desired. • Strong understanding of experimental design, regression analysis ...

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All JobsR Statistical Programmer JobsR Statistical Programmer Jobs in California

R Statistical Programmer information

See California salary details

$83.4K

$145.4K

$245.7K

How much do r statistical programmer jobs pay per year?

As of Jun 14, 2026, the average yearly pay for r statistical programmer in California is $145,363.00, according to ZipRecruiter salary data. Most workers in this role earn between $123,400.00 and $157,900.00 per year, depending on experience, location, and employer.

What is an R Statistical Programmer job?

An R Statistical Programmer is responsible for writing and optimizing code in R to analyze and manage statistical data, often in industries like pharmaceuticals, finance, or research. They develop data visualizations, automate reports, and ensure data integrity for decision-making. Many work closely with statisticians and data scientists to implement models and validate results. Strong knowledge of statistical methods, data manipulation, and regulatory requirements (in certain industries) is often required.

What are the key skills and qualifications needed to thrive in the R Statistical Programmer position, and why are they important?

To thrive as an R Statistical Programmer, you need a strong foundation in statistics, programming in R, and data analysis, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with data visualization tools, database management systems (such as SQL), and industry-relevant certifications like SAS or R programming credentials are highly valued. Strong problem-solving skills, attention to detail, and the ability to communicate complex findings clearly make a candidate stand out. These capabilities ensure accurate data-driven insights, efficient workflow, and effective collaboration within multidisciplinary project teams.

What does a typical day look like for an R Statistical Programmer?

A typical day for an R Statistical Programmer often involves writing and optimizing R scripts to analyze datasets, creating data visualizations, and collaborating with data scientists, statisticians, or project managers to deliver actionable insights. You might spend time cleaning and preparing raw data, performing statistical modeling, and documenting your methods to ensure reproducibility. Communication is key, as you'll regularly present your findings to both technical and non-technical stakeholders. Depending on the industry, you may work independently or as part of a team in academic, healthcare, finance, or technology environments.

What are the most commonly searched types of R Statistical Programmer jobs in California? The most popular types of R Statistical Programmer jobs in California are:
What are popular job titles related to R Statistical Programmer jobs in California? For R Statistical Programmer jobs in California, the most frequently searched job titles are:
What job categories do people searching R Statistical Programmer jobs in California look for? The top searched job categories for R Statistical Programmer jobs in California are:
R Statistical Programmer jobs near you
Infographic showing various R Statistical Programmer job openings in California as of June 2026, with employment types broken down into 25% As Needed, 62% Full Time, and 13% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $145,363 per year, or $69.9 per hour.

Principal Statistician, Biostatistics

Jazz Pharmaceutical

Palo Alto, CA • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

Job description

If you are a current Jazz employee please apply via the Internal Career site
Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.
Job Description
Brief Description:
The Principal Statistician, Biostatistics will be a lead statistician supporting the design and reporting of Phase I to IV clinical studies and support regulatory filings under the supervision of a more senior statistician. This role is responsible for the statistical aspects of study design, study analysis and validation, and study documentation. The Principal Statistician will provide timely and scientifically sound statistical expertise to clinical trials and develop and execute statistical strategy, design, and analyses for clinical trials. This position will work collaboratively with clinical development, pharmacology, pharmacovigilance, clinical drug supply, project management, regulatory affairs, medical writing, clinical data management, and clinical operations. The Principal Statistician will oversee work done by statistics and programming external vendors
Essential Functions
  • Participate in department and cross-functional meetings to optimize clinical study designs, endpoints, and analysis strategies.
  • Work collaboratively with members of study teams to meet study and recurring report timelines.
  • Support the development and implementation of study protocols.
  • Review and provide input to study-specific data capture systems and participate in their validation.
  • Develop statistical programs as necessary to simulate clinical trial design operating characteristics, perform analysis, prepare data displays, verify data accuracy and validity of analyses performed by statistical programming.
  • Write statistical analysis plans, perform data analysis and validation, and interpret analyses.
  • Support project lead statistician.
  • Prepare for and attend meetings with regulatory agencies.
  • Respond to statistical questions from regulatory agencies.
  • Work closely with statistical programming colleagues.
  • Monitor CRO guidelines and standards to ensure timeliness and quality of deliverables.
  • Review and validate CRO deliverables.
  • Other work as assigned by line manager.
  • Collaborate as the statistical subject matter expert with medical writers in the production of clinical reports, integrated summaries, and other documents.
  • Learn drug development regulatory requirements as they relate to statistics, including statistical contributions to marketing applications and CDISC SDTM and ADaM standards.
  • Stay current with new developments in statistics, drug development, and regulatory guidance through literature review, conference attendance, and other professional development activities.

Required Knowledge, Skills, and Abilities
  • Knowledge of clinical trial design and analysis, including experience with complex statistical methods and models, including statistical principles and methodology and principles of statistical inference, including hypothesis testing and deriving estimates, parametric and non-parametric models and techniques, principles of sample size calculations for comparing two arms, principles of design of experiments in introducing conditions designed to affect an outcome of interest, and phase II-IV clinical trial data analysis.
  • Experience in using SAS and R; knowledge of other statistical applications and programming languages a plus.
  • Knowledge of applicable regulatory requirements and guidelines, e.g., ICH Guidelines.
  • Able to work in a fast-paced, flexible, team-oriented environment.
  • Possess excellent interpersonal and communication skills (written and verbal).
  • Strong attention to detail with a view to bring studies to a quality conclusion.
  • Flexible, positive, creative thinker, good communicator.
  • Be able to work without close supervision with effective time management.

Required/Preferred Education and Licenses
  • MS or MPH in statistics, mathematics, or a related discipline with a statistical focus and > 2 years of experience in pharmaceutical or biotechnology industry.
  • PhD in statistics, mathematics, or a related discipline with a statistical focus and < 2 years of experience in the pharmaceutical or biotechnology industry.
  • Knowledge of drug development regulations pertinent to statistical analysis.
  • Bayesian and adaptive design knowledge is preferred.
  • Proficient SAS & R programming skills, understanding of CDISC models and standards.
  • Excellent writing and communication skills, demonstrated leadership abilities and excellent interpersonal skills.

#LI-Remote
Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.
FOR US BASED CANDIDATES ONLY
Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is:
$132,000.00 - $198,000.00
Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis.
At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.
The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html

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