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Assistant R Statistical Programmer Jobs in Santa Clara, CA

Apple

NAND Q&R Engineer

Cupertino, CA · On-site

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 · On-site

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

$184K - $324K/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

$150K - $277K/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 · On-site

$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 ...

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Assistant R Statistical Programmer information

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$99.2K

$173K

$292.4K

How much do assistant r statistical programmer jobs pay per year?

As of Aug 21, 2026, the average yearly pay for assistant r statistical programmer in Santa Clara, CA is $172,985.00, according to ZipRecruiter salary data. Most workers in this role earn between $146,800.00 and $187,900.00 per year, depending on experience, location, and employer.

What is the difference between Assistant R Statistical Programmer vs Data Analyst?

AspectAssistant R Statistical ProgrammerData Analyst
Required SkillsProficiency in R, basic statistical knowledge, programming skillsData manipulation, visualization, statistical analysis, often using R or Excel
Work EnvironmentClinical research, pharmaceutical, or biotech industriesBusiness, marketing, finance, healthcare sectors
CertificationsOften requires a degree in statistics, biostatistics, or related fieldsDegree in statistics, data science, or related fields; certifications like CAP or Microsoft certifications are common

While both roles involve data analysis and programming skills, the Assistant R Statistical Programmer primarily supports clinical trials and pharmaceutical research, focusing on statistical programming in R. Data Analysts work across various industries analyzing data to inform business decisions. The roles share similar educational backgrounds but differ in industry focus and specific job functions.

Are Assistant R Statistical Programmers in demand?

Assistant R Statistical Programmers are in demand due to the growing need for data analysis and statistical programming in industries like healthcare, finance, and research. Proficiency in R, along with knowledge of clinical trial processes and statistical methods, enhances job prospects in this field.

What are the most commonly searched types of R Statistical Programmer jobs in Santa Clara, CA?

The most popular types of R Statistical Programmer jobs in Santa Clara, CA are:

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For Assistant R Statistical Programmer jobs in Santa Clara, CA, the most frequently searched job titles are:

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The top searched job categories for Assistant R Statistical Programmer jobs in Santa Clara, CA are:

What cities near Santa Clara, CA are hiring for Assistant R Statistical Programmer jobs?

Cities near Santa Clara, CA with the most Assistant R Statistical Programmer job openings:

Assistant R Statistical Programmer jobs near you
Infographic showing various Assistant R Statistical Programmer job openings in Santa Clara, CA as of July 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, and 2% Contract. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $172,985 per year, or $83.2 per hour.

Sr. Statistical Programmer

Kodiak Sciences Inc

Palo Alto, CA • On-site

Full-time

Re-posted 28 days ago

Job description

Description
Kodiak Sciences Inc. is a rapidly growing, clinical-stage biopharmaceutical company dedicated to transforming ophthalmology through innovative therapeutics. Our proprietary Antibody Biopolymer Conjugate Drug (ABCD) platform integrates protein engineering, polymer chemistry, small molecule drug discovery, and advanced drug delivery technologies to address prevalent and debilitating retinal diseases with the goal of improving patient outcomes worldwide. In this fast-growing and fast-paced organization, your expertise is needed to provide support for clinical and statistical programming activities related to multiple clinical studies.
Key Responsibilities
  • Assist in the review of key study-related documents produced by other functions, e.g. Statistical Analysis Plan, Case Report Forms, Data Management Plan, Database Specifications, EDC Data Structures, DMC plans and other clinical documents
  • Write, test and validate SAS programs to produce analysis datasets, TLFs, to be included in reports for submission to regulatory agencies, publications and other communications as needed
  • May serve as a technical lead and project manager for multiple studies managing all aspects of study deliverables related to statistical and clinical programming as needed
  • Work with internal stakeholders to gather requirements and write specifications
  • Interact and communicate with Statisticians, Data Managers, Clinical Operations, Medical Monitors, Medical Writing and Medical Monitors to address programming related study deliverables
  • Write macros for reusability
  • Review and verify vendor deliverables for quality and accuracy
  • Contribute to the development review of Statistical Programming policies, standard operating procedures and other controlled documents
  • Interface with outsourcing partners and vendors

Education & Experience
  • B.S. preferably in Mathematics, statistics, computer sciences or other related field
  • 5+ years of clinical trials experience in pharmaceutical or biopharmaceutical setting or equivalent

Additional Skills
  • Thorough knowledge of the drug development and regulatory submission cycle
  • Excellent project management skills
  • Excellent communication skills
  • Able to work in a fast pace and agile environment
  • In-depth and current knowledge of regulatory requirements and guidance
  • Excellent SAS and CDISC skills
  • Proficiency in MS Word, Excel, PowerPoint, and Project

Apply