1

Associate Sas Programmer Jobs in California (NOW HIRING)

Associate Biostatistics Director

Alameda, CA · On-site

$166.50 - $236.50/hr

Strong SAS programming knowledge. * Guides the successful completion of major programs, projects and/or functions. * Leads or manages the work of others by providing guidance to subordinates or teams ...

Associate Director, Biometrics

Carlsbad, CA · On-site +1

$164K - $222K/yr

ASSOCIATE DIRECTOR, BIOMETRICS SUMMARY: The Associate Director, Biometrics is an experienced ... Proficient with SAS programming and other statistical software (e.g., R) * Proven knowledge of ...

Showing results 21-40

Associate Sas Programmer information

See California salary details

$14

$48

$78

How much do associate sas programmer jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for associate sas programmer in California is $48.36, according to ZipRecruiter salary data. Most workers in this role earn between $33.94 and $60.72 per hour, depending on experience, location, and employer.

What is an Associate SAS Programmer?

An Associate SAS Programmer is an entry-level professional who specializes in using SAS (Statistical Analysis System) software to manage, analyze, and report data. They typically assist more senior programmers and statisticians in preparing datasets, writing code, and generating statistical reports, often within industries such as healthcare, finance, or research. This role requires a good understanding of SAS programming language, attention to detail, and the ability to follow standard operating procedures. Associate SAS Programmers often work as part of a larger data or analytics team, supporting projects by ensuring data integrity and accurate analyses.

What are the typical responsibilities of an Associate SAS Programmer?

As an Associate SAS Programmer in clinical research, you will primarily be responsible for writing and validating SAS programs to analyze clinical trial data, generate tables, listings, and figures, and ensure data integrity and compliance with regulatory standards. Your daily tasks may also include collaborating closely with statisticians, data managers, and senior programmers to review requirements and resolve data issues. This role often involves learning industry best practices and becoming familiar with CDISC standards, offering a strong foundation for career advancement in clinical data programming.

What are the key skills and qualifications needed to thrive as an Associate SAS Programmer?

To thrive as an Associate SAS Programmer, you need a solid understanding of statistical analysis, data management, and proficiency in SAS programming, often supported by a degree in statistics, computer science, or a related field. Familiarity with SAS software, data visualization tools, and knowledge of regulatory requirements or CDISC standards are typically expected, and SAS certification can be an advantage. Attention to detail, problem-solving ability, and effective communication are key soft skills for this role. These skills are crucial for ensuring accurate data analysis, efficient workflow, and clear reporting in data-driven environments such as clinical research or business analytics.

What are the most commonly searched types of Sas Programmer jobs in California?

The most popular types of Sas Programmer jobs in California are:

What are popular job titles related to Associate Sas Programmer jobs in California?

For Associate Sas Programmer jobs in California, the most frequently searched job titles are:

What job categories do people searching Associate Sas Programmer jobs in California look for?

The top searched job categories for Associate Sas Programmer jobs in California are:

What cities in California are hiring for Associate Sas Programmer jobs?

Cities in California with the most Associate Sas Programmer job openings:

Infographic showing various Associate Sas Programmer job openings in California as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 29% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $100,594 per year, or $48.4 per hour.

Associate Director, Biometrics

Ionis Pharmaceuticals, Inc.

Carlsbad, CA • On-site

$165 - $223/hr

Other

Posted 15 days ago


Job description

Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases. We’re pioneers in RNA-targeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs. With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals.

At Ionis, we pride ourselves on cultivating a challenging, motivating and rewarding environment that fosters innovation and scientific excellence. We know that our success is a direct result of the exceptional talents and dedication of our employees.

With an unprecedented opportunity to change the course of human health, we look to add diverse individuals, skill sets and perspectives to our exceptional team. We continue to invest time, money and energy into making our onsite, hybrid and remote work environments a place where solid and lasting relationships are built and where our culture and employees can thrive.

We’re building on our rich history, and we believe our greatest achievements are ahead of us. If you’re passionate about the opportunity to have meaningful impact on patients in need, we invite you to apply and join us. Experience and contribute to our unique culture while you develop and expand your career!

ASSOCIATE DIRECTOR, BIOMETRICS SUMMARY:

The Associate Director, Biometrics is an experienced leadership position requiring broad knowledge and sound judgement within biostatistics. One will be responsible for the Biostatistics components of each assigned project, including study design, documents review for other functions, statistical analysis results, and oversee CRO. In each clinical development across indications, this role is contributing to therapeutic area strategy to ensure operational efficiency of Biostatistics elements and high scientific integrity.

WORK LOCATION:

This position is based in our Carlsbad, CA campus and onsite work is preferred. Remote work may be considered. Relocation assistanceisavailable for eligible candidates.

RESPONSIBILITIES:
  • Provide statistical leadership and independent guidance for assigned clinical development programs/projects, including study design, analysis, interpretation, and development strategy.
  • Serve as the statistical lead on cross-functional study and project teams and provide recommendations on complex statistical issues.
  • Lead statistical strategy and execution across assigned studies, ensuring scientific rigor, consistency, and alignment with regulatory and industry standards.
  • Design clinical trials and provide sound statistical guidance on clinical development projects
  • Write statistical section of study protocols, statistical analysis plans and study reports
  • Develop clinical trial randomization
  • Review study protocols, CRFs, database structures, study reports and annual reports
  • Lead study or project team in the review and discussion of SAP
  • Oversee CRO statistical activities and deliverables, including quality, timelines, and implementation of statistical analysis plans.
  • Maintain study documentation of statistical analyses and supportive documents
  • Other duties as assigned
REQUIREMENTS:
  • PhD degree in Statistics, Biostatistics or related field, and at least 5 years of relevant experience, or a master’s degree in Statistics, Biostatistics or related field, and at least 8 years of relevant experience
  • Proficient with SAS programming and other statistical software (e.g., R)
  • Proven knowledge of CDISC (Clinical Data Interchange Standards Consortium) standards and application of those standards to projects
  • Demonstrates advanced oral and written communication skills

Ionis offers an excellent benefits package! Follow this link for more details:Ionis Benefits

The pay scale for this position is $164,760 to $222,888

NO PHONE CALLS PLEASE. PRINCIPALS ONLY.

Ionis Pharmaceuticals, Inc. and all its subsidiaries are proud to be EEO employers.

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.

#J-18808-Ljbffr