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Statistical Programmer Ii Jobs in California (NOW HIRING)

Pharmapace, Inc.

Senior Statistician

San Diego, CA · On-site

$100 - $165/hr

Provide input to statistical programmers to prepare CDISC compliant SDTM and ADaM datasets ... Master's degree with 4+ years or Doctoral degree with 2+ years of relevant experience in a health ...

PTI Technologies

Manufacturing Engineer II

Oxnard, CA · On-site

$79K - $132K/yr

Join PTI Technologies as a Manufacturing Engineer II and dive into the dynamic world of the ... By applying statistical methods, you'll help predict future manufacturing requirements, ensuring ...

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Showing results 21-40

All JobsStatistical Programmer Ii JobsStatistical Programmer Ii Jobs in California

Statistical Programmer Ii information

See California salary details

$83.4K

$145.4K

$245.7K

How much do statistical programmer ii jobs pay per year?

As of Aug 22, 2026, the average yearly pay for statistical programmer ii 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 is a statistical programmer ii?

Statistical Programmer IIs are professionals who use specialized software to analyze and manage large datasets, typically in clinical research or pharmaceutical settings. They are responsible for programming and validating statistical analyses, generating tables, listings, and figures, and ensuring data accuracy for regulatory submissions. This role requires proficiency in programming languages such as SAS or R, strong analytical skills, and a good understanding of clinical trial processes. Statistical Programmer IIs often work as part of a team, collaborating with statisticians and data managers to deliver high-quality data outputs.

What are the key skills and qualifications needed to thrive as a statistical programmer ii?

A Statistical Programmer II typically requires strong programming skills in SAS or R, experience with clinical trial data, and a relevant degree in statistics, mathematics, or computer science. Familiarity with CDISC standards, data management systems, and regulatory submission requirements is often expected. Attention to detail, problem-solving abilities, and effective communication are vital soft skills for collaborating with cross-functional teams and ensuring data integrity. These competencies help deliver accurate analyses and support regulatory compliance in clinical research environments.

What are some common challenges faced by a statistical programmer ii when collaborating with clinical project teams?

As a Statistical Programmer II, one common challenge is aligning the programming deliverables with the evolving needs of clinical project teams, especially when study protocols or analysis plans change. Effective communication is essential to clarify requirements and timelines with statisticians, data managers, and clinical researchers. Additionally, ensuring data quality and consistency across multiple studies while adhering to regulatory standards can be demanding. Proactively addressing these challenges with strong collaboration and attention to detail helps ensure successful project outcomes.

What is the difference between Statistical Programmer Ii vs Data Analyst?

AspectStatistical Programmer IiData Analyst
Required CredentialsBachelor's in Statistics, Computer Science, or related field; programming skills in SAS, R, or PythonBachelor's in Statistics, Data Science, or related field; proficiency in Excel, SQL, and visualization tools
Work EnvironmentPharmaceutical or clinical research settings, working with clinical trial dataBusiness, healthcare, or marketing sectors analyzing large datasets
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsCorporations, healthcare providers, market research firms

While both roles involve data analysis, Statistical Programmer Ii primarily focuses on programming and preparing clinical trial data, whereas Data Analysts interpret data to inform business decisions. The roles share similar educational backgrounds and technical skills but differ in industry focus and daily tasks.

What are popular job titles related to Statistical Programmer Ii jobs in California?

For Statistical Programmer Ii jobs in California, the most frequently searched job titles are:

What job categories do people searching Statistical Programmer Ii jobs in California look for?

The top searched job categories for Statistical Programmer Ii jobs in California are:

Statistical Programmer Ii jobs near you
Infographic showing various Statistical Programmer Ii job openings in California as of August 2026, with employment types broken down into 84% Full Time, and 16% Part Time. Highlights an 100% In-person job distribution, with an average salary of $145,363 per year, or $69.9 per hour.

Senior Manager, Statistical Programming - Oncology Early Development

AbbVie

South San Francisco, CA • On-site

$104K - $128K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 20 days ago

AbbVie rating

8.6

Company rating: 8.6 out of 10

Based on 101 frontline employees who took The Breakroom Quiz

15th of 86 rated pharmaceutical

Job description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

The Senior Manager, Statistical Programming performs statistical programming and analysis oversight for

OED (Oncology Early Development) clinical projects conducted by CROs. This individual is responsible for

overseeing several compounds/indications on all statistical programming related tasks delivered by CROs.

The goal is to ensure data integrity and high quality of all the analysis for oncology first in human clinical

trials up through clinical proof of concept. This individual also performs hands on programming to validate

analysis datasets and TLFs delivered by CRO and support in-house studies for full set of analysis tasks. This

individual may need to manage other regular or contract statistical programmers.

Responsibilities:

•Leads the statistical programming activities for one or more compounds/indications or a therapeutic

area.

•Manages a team of statistical programmers and the resource planning for their assigned projects.

•Ensures timely deliverables, that all quality processes are followed and consistency within the

projects.

•Develops and oversees the development of SAS programs for the creation of ADaM data sets

following CDISC standards.

•Develops and oversees the development of SAS programs for the creation of Tables, Listings and

Figures.

•Ensures consistency of ADaM data sets for individual studies and integrated data.

•Creates documentation for regulatory filings including reviewers guides and data definition

documents.

•Leads the development of standard SAS Macros and the development of standard operating

procedures.

•Manages, mentors and creates career development plans for assigned staff.

•Participates in the recruitment and selection of new staff.

Qualifications

•MS in Statistics, Computer Science or a related field with 9+ years of relevant experience. OR BS in

Statistics, Computer Science or a related field with 11+ years of relevant experience.

•Minimum of 2 years experience leading a team of statistical programmers.

•In-depth understanding of SAS programming concepts and techniques related to drug development.

•In-depth understanding of CDISC Standards.

•In-depth understanding of the drug development process, including experience with regulatory

filings.

•Ability to communicate clearly both oral and written.

•Ability to effectively represent the Statistical Programming Organization in cross functional teams.

•Ability to accurately estimate effort required for project related programming activities.


Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of thisposting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​

  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​

  • This job is eligible to participate in our long-term incentive programs. ​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

What AbbVie employees say

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

View All AbbVie Jobs