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Senior Statistical Programmer Jobs in California

Jazz Pharmaceutical

Sr Principal Statistician

Palo Alto, CA · On-site

$102K - $125K/yr

The Senior Principal Statistician will provide timely and scientifically sound statistical ... Experience in using SAS and R; knowledge of other statistical applications and programming ...

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All JobsSenior Statistical Programmer JobsSenior Statistical Programmer Jobs in California

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 17, 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:
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What are popular job titles related to Senior Statistical Programmer jobs in CA? For Senior Statistical Programmer jobs in CA, the most frequently searched job titles are:
Senior Statistical Programmer jobs near you
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. Principal Analyst, Statistical Programming

Sr. Principal Analyst, Statistical Programming

Neurocrine Biosciences, Inc.

San Diego, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 4 days ago

Job description

Who We Are:
At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs.
What We Do:
Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis* and uterine fibroids,* as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X and Facebook. (*in collaboration with AbbVie)
About the Role:
Leads major statistical programming efforts for clinical program area of responsibility. Develops and recommends system capabilities roadmap for in-house development and external vendor selection process. Acts as a system expert in designing, developing, testing, maintaining, validating, and documenting SAS programs to evaluate clinical data and meet the project requirements for SAS statistical programming efforts. Provides expert-level technical advice for all aspects of the program development process, tools and software, standards and procedures.
Your Contributions (include, but are not limited to):
  • Provides expert technical leadership across multiple functions serving as the key representative for Biometrics
  • Contributes to the development of Biometrics functional strategy and serves as system expert for Statistical Programming efforts
  • Leads and mentors a team of statistical programmers to support the analysis and reporting of data from clinical and nonclinical studies for all corporate development programs
  • Leads end-to-end statistical programming work-streams on multidisciplinary program teams company-wide
  • Provides technical direction in the development and implementation of programming standards and conventions, building statistical programming infrastructure
  • Provides workforce planning recommendations based on project workloads in order to ensure appropriate programming resources are available to complete tasks in a timely manner
  • Manages vendor selection processes and validates vendor programming activities such as CDISC implementation, analysis reporting, and programming conventions
  • Supports creation and validation of e-submission requirements (i.e. annotated CRF, datasets files, define documents)
  • Serves as primary/lead programmer for agency reporting deliverables such as DSUR/Annual Report and IB updates
  • Performs the function of lead and/or quality control statistical programmer on projects as needed
  • Performs other duties as assigned
Requirements:
  • BS/BA degree in computer science, mathematics, statistics, or related discipline AND 8+ years in the Biopharmaceutical (or CRO) industry as a statistical programmer with advanced knowledge of SAS, (Base, Stat, Macro, graph), CDISC data structures. In addition, must have at least 2 years of experience serving in a supervisory or lead capacity. Experience managing large projects and external vendors. OR
  • Master's degree in computer science, mathematics, statistics, or related discipline AND 6+ years similar experience noted above OR
  • PhD degree in computer science, mathematics, statistics, or related discipline AND 4+ years similar experience noted above
  • Anticipates business and industry issues; recommends relevant process / technical / service improvements
  • Demonstrates broad expertise or unique knowledge
  • Considered an expert within the company and may have external presence in area of expertise
  • Applies in-depth expertise in discipline and broad knowledge of other closely related areas to improve efficiency of team
  • Ability to work as part of and lead multiple teams
  • Good leadership, mentoring skills and abilities typically leads lower levels and/or indirect teams
  • Excellent computer skills
  • Excellent communications, problem-solving, analytical thinking skills
  • Sees broader picture and longer-term impact on division/company
  • Ability to meet multiple deadlines across a variety of projects/programs, with a high degree of accuracy and efficiency
  • Excellent project management, strong project leadership skills
  • Expert knowledge of the following:
    • Developing and implementing statistical programming SOPs and processes in a clinical environment
    • Relational databases and complex data systems.
    • Industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines
    • Programming skills in SAS, (Base, Stat, Macro, graph), R, STAT or similar
    • SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domains
  • Knowledge of all aspects of writing, validating, and documenting statistical programs, and of creating integrated programming libraries and systems
  • Proven experience in multi-discipline, cross-functional project management in a clinical, highly regulated environment
  • Track record of success with effectively organizing and managing multiple assignments with challenging timelines across multiple personnel

#LI_SA1
Neurocrine Biosciences is an EEO/Disability/Vets employer.
We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.
The annual base salary we reasonably expect to pay is $156,900.00-$214,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.

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