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Senior Statistical Programmer Analyst information

See California salary details

$81.4K

$126.6K

$165.3K

How much do senior statistical programmer analyst jobs pay per year?

As of Jul 18, 2026, the average yearly pay for senior statistical programmer analyst 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 are the key skills and qualifications needed to thrive as a Senior Statistical Programmer Analyst, and why are they important?

To thrive as a Senior Statistical Programmer Analyst, you need advanced programming skills in SAS or R, a strong background in statistics, and a relevant degree such as in mathematics, statistics, or computer science. Experience with clinical trial data, CDISC standards (SDTM, ADaM), and regulatory submission processes, along with certifications like SAS Certified Professional, are highly valued. Exceptional problem-solving abilities, attention to detail, and effective communication enable you to manage complex datasets and collaborate with cross-functional teams. These combined skills ensure accurate data analysis, regulatory compliance, and successful delivery of biostatistical projects in the pharmaceutical or clinical research industry.

What does a Senior Statistical Programmer Analyst do?

A Senior Statistical Programmer Analyst is responsible for designing, developing, and validating statistical programs that analyze clinical trial or research data. They work closely with biostatisticians and data managers to ensure data accuracy, integrity, and compliance with regulatory standards. Their work includes creating tables, listings, and figures (TLFs), developing analysis datasets, and automating data processes. Senior Statistical Programmer Analysts often mentor junior programmers and play a key role in quality control and project delivery within pharmaceutical, biotechnology, or clinical research organizations.

How does a Senior Statistical Programmer Analyst typically collaborate with cross-functional teams in clinical research projects?

As a Senior Statistical Programmer Analyst, you will regularly collaborate with biostatisticians, data managers, clinical research associates, and project managers. Your main responsibility is to translate statistical analysis plans into programming code (often using SAS or R), ensuring datasets and outputs meet regulatory standards. You’ll participate in team meetings to clarify study requirements, address data or programming issues, and ensure timelines are met. Strong communication and documentation skills are essential, as you often serve as a bridge between technical and non-technical team members.
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Senior Statistical Programmer Analyst jobs near you
Sr. Statistical Programmer

Sr. Statistical Programmer

Kodiak Sciences Inc.

Palo Alto, CA • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job 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