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Associate Statistical Programmer Jobs in California

Jj

Associate Director of Stats Programming

Irvine, CA · On-site

Learn more at We are searching for the best talent for an Associate Director of Stats Programming ... SOP), Statistical Analysis Systems (SAS) Programming The anticipated base pay range for this ...

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How much do associate statistical programmer jobs pay per year?

As of Jun 1, 2026, the average yearly pay for associate 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 are the key skills and qualifications needed to thrive as an Associate Statistical Programmer, and why are they important?

To thrive as an Associate Statistical Programmer, you need a solid background in statistics, programming (especially SAS or R), and familiarity with clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Proficiency with statistical software (such as SAS, R, or Python), CDISC standards, and data management tools is essential, and certifications in SAS programming can be advantageous. Attention to detail, strong problem-solving abilities, and effective communication skills help you collaborate with clinical teams and ensure data quality. These skills and qualities are vital for delivering accurate statistical analyses that support regulatory submissions and evidence-based decision-making in clinical research.

How does an Associate Statistical Programmer typically collaborate with biostatisticians and data managers in clinical research projects?

As an Associate Statistical Programmer, you will frequently collaborate with biostatisticians to understand statistical analysis plans and translate them into clear programming specifications. You’ll also work closely with data managers to ensure data integrity and resolve any data discrepancies before analysis. Effective communication and teamwork are essential, as you’ll often participate in project meetings, provide programming support, and help deliver high-quality datasets and reports under tight timelines. This collaborative environment is key to ensuring accurate and timely clinical trial results.

What is an Associate Statistical Programmer?

An Associate Statistical Programmer is an entry-level professional who assists in the programming and analysis of clinical trial data, primarily within the pharmaceutical or biotechnology industries. They use statistical software, such as SAS or R, to create, validate, and maintain datasets, tables, listings, and figures required for clinical study reports. Their work supports biostatisticians and clinical teams in ensuring data accuracy and regulatory compliance. This role is ideal for those with a background in statistics, mathematics, or computer science, looking to start a career in clinical data analysis.

What is the difference between Associate Statistical Programmer vs Statistical Programmer?

AspectAssociate Statistical ProgrammerStatistical Programmer
Required CredentialsBachelor's degree in statistics, mathematics, or related field; some roles may require basic programming skillsBachelor's or master's degree; more experience in programming and statistical analysis
Work EnvironmentEntry-level, supporting senior programmers; often in clinical research or pharmaceutical companiesMore independent, handling complex analyses; similar industry settings
Employer & Industry UsageCommon in clinical trials, pharmaceutical, and biotech companiesUsed across similar industries, often as a step up from associate roles

The main difference between an Associate Statistical Programmer and a Statistical Programmer lies in experience and responsibility level. Associate roles are typically entry-level, focusing on supporting tasks under supervision, while Statistical Programmers handle more complex analyses independently. Both roles are vital in clinical research and biotech industries, with the associate position serving as a stepping stone to more advanced programming roles.

What are the most commonly searched types of Statistical Programmer jobs in California? The most popular types of Statistical Programmer jobs in California are:
What are popular job titles related to Associate Statistical Programmer jobs in California? For Associate Statistical Programmer jobs in California, the most frequently searched job titles are:
What job categories do people searching Associate Statistical Programmer jobs in California look for? The top searched job categories for Associate Statistical Programmer jobs in California are:
What cities in California are hiring for Associate Statistical Programmer jobs? Cities in California with the most Associate Statistical Programmer job openings:
Associate Statistical Programmer jobs near you
Infographic showing various Associate Statistical Programmer job openings in California as of May 2026, with employment types broken down into 1% Internship, 10% As Needed, 87% Full Time, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $145,363 per year, or $69.9 per hour.
Associate Director, Statistical Programming

Associate Director, Statistical Programming

Revolution Medicines

Redwood City, CA • Hybrid

Other

Posted 18 days ago

Job description

The Opportunity:

Position requires 14+ years of Statistical Programming experience with exploratory-stage oncology clinical trials, providing programming support and oversight of one or more clinical programs (early or late phase) within Statistical Programming function. In addition to hands-on Programming, this position requires providing oversight and programming support and guidance for internal deliverables and regulatory submissions while ensuring conformance to CDISC standards and submission guidelines. Based on company needs, this position will be required to lead one or more early Phase or late phase studies/programs. Specific responsibilities include:

  • Effective collaborating with cross functional teams to provide programming timelines for various deliverables.

  • Provide SAS Programming technical support and guidance to programming team.

  • Oversight/participation in any internal/mock or regulatory authority audits.

  • Timeline and vendor management for deliverables, including submission-related activities,  complying with regulatory standards (e.g., FDA 21 CFR Part 11, GxP).

  • Oversee the programming support for relevant deliverables, such as Investigator Brochures, publications, US and ex-US regulatory submissions, including CDISC compliant datasets (SDTM, ADaM) and data documentation, Reviewer's Guide, TLFs, Statistical Analysis Plans (study specific, ISS, ISE, Exposure-Response), blank and annotated CRFs, and actual patient CRFs.

  • Hands-on programming and management of in-house deliverables including but not limited to Dose Committee meetings, Board of Director meetings, Exploratory Analysis, etc.

  • Oversight and Verification Review of documents, spreadsheets, slides for in-house presentations and external publications.

Titles may vary based on candidate experience.

Required Skills, Experience and Education:

  • 14+ years of Statistical Programming experience with early or late phase oncology trial studies.

  • BS/BA degree or other suitable qualification with relevance to the field.

  • Experience leading one or more statistical programming contractors, and programming vendors.

  • Proficiency in providing hands-on SAS Programming support for production or validation of analysis datasets, tables, listings and figures.

  • Demonstrated ability to multi-task, prioritize options, anticipate challenges, and execute goals as a member of an interdisciplinary team is extremely important.

Preferred Skills:

  • A demonstrable record of strong leadership and teamwork.

  • Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high energy environment.

  • Experience working in a small to mid sized biotech/pharma environment.

  • Experience collaborating on development of processes, SOPs and guidance documents for the Statistical Programming function. 

    #LI-Hybrid  #LI-DN1

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