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Associate Statistical Programmer Jobs in Fremont, CA

MEDVACON

Research Associate - pharma

Foster City, CA · On-site

... statistical programming languages such as R and Python is a plus. Additional Information Vaccine mandate is in effect due to onsite nature of the position Please attach a WORD resume to your ...

MEDVACON

Research Associate - pharma

Foster City, CA

Experience with Microsoft Word and Excel is essential, and knowledge in statistical programming ... NOTE - other temporary roles with this company: 2 Research Associate in Santa Monica, CA 1 Clinical ...

Exelixis

Associate Biostatistics Director

Alameda, CA · On-site

$166K - $236K/yr

Works collaboratively with clinicians, data managers, biostatisticians, statistical programmers, and medical writers in the planning, conduct and analysis of clinical trials. Essential Duties And ...

Exelixis

Associate Biostatistics Director

Alameda, CA · On-site

$166K - $236K/yr

Works collaboratively with clinicians, data managers, biostatisticians, statistical programmers, and medical writers in the planning, conduct and analysis of clinical trials. Essential Duties And ...

Exelixis

Associate Biostatistics Director

Alameda, CA · On-site

$166K - $236K/yr

Works collaboratively with clinicians, data managers, biostatisticians, statistical programmers, and medical writers in the planning, conduct and analysis of clinical trials. Essential Duties And ...

Exelixis Inc

Associate Biostatistics Director

Alameda, CA · On-site

$166.50 - $236.50/hr

Works collaboratively with clinicians, data managers, biostatisticians, statistical programmers, and medical writers in the planning, conduct and analysis of clinical trials. Responsibilities * Work ...

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Showing results 21-40

All JobsAssociate Statistical Programmer JobsAssociate Statistical Programmer Jobs in Fremont, CA

Associate Statistical Programmer information

See Fremont, CA salary details

$92.5K

$161.2K

$272.6K

How much do associate statistical programmer jobs pay per year?

As of Sep 4, 2026, the average yearly pay for associate statistical programmer in Fremont, CA is $161,235.00, according to ZipRecruiter salary data. Most workers in this role earn between $136,800.00 and $175,100.00 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 Fremont, CA?

The most popular types of Statistical Programmer jobs in Fremont, CA are:

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For Associate Statistical Programmer jobs in Fremont, CA, the most frequently searched job titles are:

What job categories do people searching Associate Statistical Programmer jobs in Fremont, CA look for?

The top searched job categories for Associate Statistical Programmer jobs in Fremont, CA are:

What cities near Fremont, CA are hiring for Associate Statistical Programmer jobs?

Cities near Fremont, CA with the most Associate Statistical Programmer job openings:

Associate Statistical Programmer jobs near you
Infographic showing various Associate Statistical Programmer job openings in Fremont, CA as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 25% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $161,235 per year, or $77.5 per hour.

Associate Director Oncology Biostatistics

Penfield Search Partners

San Francisco, CA • On-site

Full-time

Re-posted 17 days ago

Key responsibilities

  • Develop and execute statistical strategies for clinical trials across all phases.

  • Collaborate with cross-functional teams to plan, conduct, analyze, and report clinical trial data.

  • Review and oversee the programming of ADaMs and TLFs, and ensure high-quality deliverables within timelines.

Job description

Job Description Our client is a clinical-stage biopharma company focusing in the Oncology space. They are currently seeking a highly skilled and experienced Associate Director of Biostatistics to provide leadership to develop and execute statistical strategy, design and analyses for clinical trials in all phases. As Associate Director you will apply sound statistical methodology to meet project objectives, health authority guidelines, and regulatory requirements.

This is an onsite role based in the Bay Area. Apply extensive technical expertise and experience to provide written and verbal recommendations on statistical issues, design and conduct of clinical trials of all phases. Use initiative to develop, maintain and share knowledge of the theory and application of current statistical methods appropriate for data analysis and clinical trial design.

Work collaboratively with clinicians, data managers, biostatisticians, statistical programmers, and medical writers in the planning, conduct and analysis of clinical trials. Work with project team members on developing clinical protocol. Review CRFs, CRF edit checks and CRF completion guidelines.

Author statistical analysis plan, TLF shells and Table of contents for outputs to be generated. Review ADaM specifications and verify primary and secondary efficacy endpoints. Perform analysis, interpret study results, and collaborate with clinical team to produce interim reports, final reports, and publications.

Effectively manage CRO to ensure high-quality deliverables within timeline and budget. Oversee programming of ADaMs and TLFs for the study. Responsible for one or more studies with concurrent tasks and timelines.

Participate in the validation/QC of key study endpoint analysis and submission deliverables. Apply appropriate regulatory guidelines to the projects. Guide the successful completion of major programs, projects and/or functions.

Develop technical and/or business solutions to complex problems. Identify and implement methods, techniques, procedures, and evaluation criteria to achieve results. Performs a variety of complicated tasks with a wide degree of creativity and latitude.

Please Have: MS/MA degree in related discipline and a minimum of 9 years of related experience; or, PhD in related discipline and a minimum of 5 years of related experience; or, Experience in Oncology and study Phases I-III highly preferred. Experience in Biotech/Pharmaceutical industry preferred. Experience with managing CROs in the conduct of clinical trials.

Experience with statistical applications and clinical data management procedures in the conduct of clinical trials. Ability to effectively represent Biostatistics and Clinical Data Management in multidisciplinary meetings. Knowledge of appropriate regulations, industry standards and guidance documents.

Ability to interact effectively with biostatistical, data management, operations, and clinical personnel from CROs and companies collaborating with Exelixis. Developed/reviewed SDTM/ADaM specifications Strong SAS programming knowledge. Complete understanding and wide application of technical principles, theories, concepts, and techniques.

Have good general knowledge of other related disciplines.

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