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Associate Statistical Programmer information

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$83.4K

$145.4K

$245.7K

How much do associate statistical programmer jobs pay per year?

As of Aug 21, 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 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.

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 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.

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 August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 23% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $145,363 per year, or $69.9 per hour.

Associate Statistical Analyst (on-site)

Abbott

Santa Clara, CA • On-site

$77K - $126K/yr

Full-time

Medical, Retirement

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

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

175th of 543 rated manufacturers

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year An excellent retirement savings plan with high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree. A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. The Opportunity We are seeking an Associate Statistical Analyst to join our Clinical Research team for Abbott Medical Devices on-site in Santa Clara, CA. In this role, the Associate Statistical Analyst will provide statistical support to the Biostatistics Supervisor/Manager and the Cardiovascular Division (CVD) for clinical studies. This includes assisting with the review of table mockups, CRFs and edit check specifications; work with biostatisticians to validate data tables, figures and listings; write and document programs; assist in ad hoc programming; and assist in QC. What You'll Work On Assist with QC and validation of tables, listings, figures based on table specifications. QC summary statistics in presentation slides and clinical reports against validated tables, figures, listings. Assist with the review of CRF, edit checks, and table mock-ups and provide comments to lead statistician/ Statistical Analyst. Independently modify existing table programs. Assist in creating data listing or summary to Data Management for data cleaning. Assist in documentation of programs and specification documents. Demonstrate basic knowledge of SAS data steps, procedures and macros. Be able to use existing macros. Provide accurate and timely answers to routine questions. Communicate an understanding of basic clinical principles for his/her project and acts in accordance with those principles. Inform supervisor or manager on important issues in a timely manner. Required Qualifications Associate's degree. Minimum 1 year of experience. Preferred Qualifications Master's degree or PhD 2 years' experience in medical device or pharmaceutical clinical research studies. Statistical knowledge and SAS skills (i.e., proven experience in SAS coding). Experience working on medical device clinical studies in highly regulated environment. Ability to work within a team and as an individual contributor in a fast-paced, changing environment. Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization. Multitasks, prioritizes and meets deadlines in timely manner. Strong organizational skills, attention to detail, and financial/business acumen Abbott is an Equal Opportunity Employer, committed to employee diversity. The base pay for this position is $77,600.00 – $126,700.00. In specific locations, the pay range may vary from the range posted. #J-18808-Ljbffr

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