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Associate Director Statistical Programming Jobs in California

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Associate Director Statistical Programming information

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$151.5K

$276.5K

$339.5K

How much do associate director statistical programming jobs pay per year?

As of Jul 14, 2026, the average yearly pay for associate director statistical programming in California is $276,479.00, according to ZipRecruiter salary data. Most workers in this role earn between $257,100.00 and $318,300.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Associate Director Statistical Programming, and why are they important?

To thrive as an Associate Director Statistical Programming, you need expertise in statistical programming, clinical trial data standards, and a degree in statistics, mathematics, or a related field, often with several years of experience in the pharmaceutical or biotechnology industry. Proficiency in programming languages such as SAS and R, knowledge of CDISC standards (SDTM, ADaM), and familiarity with regulatory submission requirements are typically required. Strong leadership, project management, and communication skills are vital for guiding teams and collaborating with cross-functional partners. These skills and qualities ensure the delivery of high-quality, compliant statistical outputs that support clinical development and regulatory approval.

What does an Associate Director of Statistical Programming do?

An Associate Director of Statistical Programming leads teams responsible for the design, development, and validation of statistical programs used in the analysis of clinical trial data. They oversee the creation of datasets, tables, listings, and figures that support regulatory submissions and scientific publications. In addition to technical expertise, this role involves managing timelines, ensuring compliance with regulatory standards, and collaborating with cross-functional teams such as biostatistics, data management, and clinical operations.

How does an Associate Director of Statistical Programming typically collaborate with cross-functional teams in a pharmaceutical or biotech setting?

As an Associate Director of Statistical Programming, you will work closely with biostatisticians, clinical data managers, and regulatory affairs professionals to ensure that statistical analyses and data outputs meet project and regulatory requirements. You’ll often lead programming teams, coordinate timelines, and help translate statistical analysis plans into executable code. Regular meetings and clear communication are key, as you’ll be expected to provide technical guidance and ensure data integrity across multiple studies or programs. This role often requires balancing hands-on programming with strategic leadership and mentorship responsibilities.

What is the difference between Associate Director Statistical Programming vs Statistical Programmer?

AspectAssociate Director Statistical ProgrammingStatistical Programmer
Required CredentialsBachelor's or Master's in Biostatistics, Statistics, or related field; experience in clinical trial programmingBachelor's or Master's in similar fields; entry to mid-level experience
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPerforms programming tasks, supports project teams, executes statistical analyses
Employer & Industry UsagePharmaceutical and biotech companies, clinical research organizationsPharmaceutical companies, CROs, biotech firms

The Associate Director Statistical Programming typically oversees programming teams and manages project deliverables, requiring leadership skills and extensive experience. In contrast, the Statistical Programmer focuses on executing programming tasks under supervision. Both roles are essential in clinical research, but the Associate Director holds more managerial responsibilities and strategic oversight.

What are popular job titles related to Associate Director Statistical Programming jobs in California? For Associate Director Statistical Programming jobs in California, the most frequently searched job titles are:
What job categories do people searching Associate Director Statistical Programming jobs in California look for? The top searched job categories for Associate Director Statistical Programming jobs in California are:
What cities in California are hiring for Associate Director Statistical Programming jobs? Cities in California with the most Associate Director Statistical Programming job openings:
Associate Director Statistical Programming jobs near you
Associate Director, Biostatistics Clinical Late Stage

Associate Director, Biostatistics Clinical Late Stage

Revolution Medicines

Redwood City, CA • Hybrid

Other

Posted 13 days ago

Job description

The Opportunity:

This position serves as a study level statistician for oncology studies in clinical late-stage development and provides leadership across biostatistical activities. The Associate Director will collaborate across functions and contribute to program-level decision-making.  

  • Represent biostatistics on study and cross-functional project teams, providing statistical leadership

  • Lead and manage biostatistical activities to ensure consistency, scientific rigor, and timely deliverables.

  • Provide statistical expertise for design, analysis and reporting of clinical studies.

  • Develop statistical analysis plans and analysis specifications; ensure analyses align with clinical and regulatory objectives.

  • Collaborate with statistical programming to ensure that analysis is conducted per statistical plan and specifications and delivered with high quality.

  • Collaborate with data management and clinical operations to ensure robust CRF and database development and quality data collection.

  • Provide statistical input to the development of global health authority documents, regulatory interaction, and response to health authority submissions.

  • Influence strategy and inform decision-making through data-driven insights and clear communication of risk and benefit.

  • Collaborate in publications, assist in data interpretation, and ensure consistency and accuracy in data presentation.

  • Contribute to the development of functional-level standards, SOPs, and templates.

  • Keep abreast in new developments in statistics, drug development, and regulatory guidance and share knowledge with functional and cross-functional team members.

Required Skills, Experience and Education:

  • Ph.D. or M.S. in Statistics/Biostatistics, a minimum of 5 years (for Ph.D.) and 8 years (for M.S.) of experience in biotech/pharma industry as a statistician. Level will be determined based on the relevance of experience.

  • Hands-on experience in design and analysis of late-stage oncology trials is a must.

  • Ability to work independently and within a team.

  • Solid knowledge in ICH and other regulatory requirements related to biostatistical activities and clinical trials.

  • Excellent verbal and written communication skills are required.

  • Good interpersonal and project management skills are essential.

  • Proficiency in SAS and/or R.

Preferred Skills:

  • Hands-on experience in design and analysis of phase 3 oncology trials is desirable.

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