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Senior Statistical Programmer Jobs in California

Perform the role of the Lead Statistical Programmer. * Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget ...

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Senior Statistical Programmer information

See California salary details

$81.4K

$126.6K

$165.3K

How much do senior statistical programmer jobs pay per year?

As of Jun 15, 2026, the average yearly pay for senior statistical programmer in California is $126,613.00, according to ZipRecruiter salary data. Most workers in this role earn between $105,600.00 and $146,100.00 per year, depending on experience, location, and employer.

What is a Senior Statistical Programmer job?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

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

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

What are the typical responsibilities and team dynamics for a Senior Statistical Programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.

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 job categories do people searching Senior Statistical Programmer jobs in California look for? The top searched job categories for Senior Statistical Programmer jobs in California are:
What cities in California are hiring for Senior Statistical Programmer jobs? Cities in California with the most Senior Statistical Programmer job openings:
Infographic showing various Senior Statistical Programmer job openings in California as of June 2026, with employment types broken down into 20% As Needed, 20% Full Time, 20% Part Time, and 40% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $126,613 per year, or $60.9 per hour.
Sr. Statistical Programmer

Other

Posted 19 days ago


Job description

SUMMARY:

A biopharmaceutical company in the Bay area needs a very strong Senior Statistical Programmer to support their team. This programmer will need to be a strong, senior-level programmer who can work well both independently and part of a team. They must be proficient in their CDISC expertise and be able to program specifications from scratch (both SDTM and ADaM programming).


DUTIES & RESPONSIBILITIES:

  • Perform data manipulation, analysis and reporting of clinical trial data
  • Program and generate tables, listings, and graphs (TLGs)
  • Participate in the review of statistical analysis plans, table specification, develop specification for SDTM and ADaM data sets.
  • Review, and comment on CRFs, annotated CRFs, and edit checks and related documents.
  • Participate in study team meetings and address issues that may affect statistical programming.
  • Validate and document SAS programs and output
  • Create SDTM and ADaM Datasets and related documentation
  • Fulfill ad-hoc programming requests
  • Other duties as needed


QUALIFICATIONS & REQUIREMENTS:

  • 15+ years of statistical programming experience in the pharmaceutical/biotech industries, good tenure with Sponsor companies
  • Strong submissions experience (BLA, NDA/sNDA and EMA), understanding submission requirements, and end to end programming experience
  • Strong experience with CDISC implementation – SDTM/ADAM, must be able to develop specifications from scratch
  • Demonstrated ability performing all levels of programming activities for a clinical project
  • Experience working in the Cardiovascular or Neuromuscular areas is a plus