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Associate Director Statistical Programming Jobs in California

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Associate Director Statistical Programming information

See California salary details

$151.5K

$276.5K

$339.5K

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

As of Jun 19, 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.

How to become a director of statistical programming?

To become a director of statistical programming, professionals typically need extensive experience in statistical programming, often 8-10 years, with a strong background in biostatistics, data analysis, and programming languages like SAS or R. Advancing usually requires demonstrating leadership skills, managing teams, and understanding regulatory requirements; obtaining relevant certifications and a master's or doctoral degree can also support career progression.

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.

Is an associate director a high level position?

An Associate Director in statistical programming is considered a senior-level position within an organization, often responsible for overseeing project teams, managing timelines, and ensuring regulatory compliance. It typically requires several years of experience and advanced skills in programming languages like SAS or R, along with leadership abilities. This role is generally regarded as a high-level management position in the industry.

How much does a statistical programmer earn?

A statistical programmer's salary varies based on experience, location, and industry, but typically ranges from $70,000 to $120,000 annually. Senior roles or those with specialized skills in programming languages like SAS or R can earn higher salaries, especially in the pharmaceutical or biotech sectors.

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.

How much does a Pfizer statistical programming manager make?

A Pfizer statistical programming manager typically earns between $120,000 and $160,000 annually, depending on experience, location, and level within the company. Compensation may also include bonuses and benefits, and strong skills in SAS, R, or Python are often required for the role.

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:
Infographic showing various Associate Director Statistical Programming job openings in California as of June 2026, with employment types broken down into 100% Full Time. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $276,479 per year, or $132.9 per hour.
Assoc Director, Statistical Programming

Assoc Director, Statistical Programming

Gilead

Foster City, CA • On-site

$195K - $253K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Posted 3 days ago


Gilead Sciences rating

9.7

Company rating: 9.7 out of 10

Based on 7 frontline employees who took The Breakroom Quiz

1st of 71 rated pharmaceutical


Job description

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
Job Description

Associate Director, Statistical Programming

(Macro Support)

Job Summary

Leads statistical programming tool development (e.g., SAS macros, automation solutions) supporting multiple studies and/or workstreams and ensuring delivery of high-quality, scalable tools aligned with Clinical Data Science and Statistical Programming standards. Contributes to departmental strategies, tools, and infrastructure that enable efficiency and consistency across Statistical Programming.

Key Responsibilities

Leadership & Delivery

  • Accountable for planning and delivery of tool development aligned with study and business timelines.

  • Influences design, development, qualification, and maintenance of SAS macros and related tools used across multiple studies or initiatives.

  • Acts as a project or functional lead for statistical programming tool initiatives.

  • Identifies cross-project synergies to improve efficiency, consistency, and reuse of tools and processes.

Technical & Functional Expertise

  • Maintains advanced knowledge of statistical programming good practices, data standards and norms.

  • Designs and develops tools in SAS Macro (required); familiarity with Linux scripting, R, or Python preferred.

  • Ensures tools comply with Gilead systems development procedures and regulatory requirements.

  • Drives adoption of standardized programming tools, templates, and methodologies following documented workflows.

  • Anticipates and resolves technical challenges, providing guidance to team members.

  • Provides primary and secondary tool development support as needed.

Strategy & Continuous Improvement

  • Contributes to development of departmental strategies, standards, and infrastructure for statistical programming tools.

  • Leads or contributes to initiatives that improve efficiency, automation, and scalability across programming workflows.

  • Evaluates and recommends new tools, processes, or technologies to enhance productivity and data flow.

Collaboration & Influence

  • Represents Clinical Data Engineering and Macro Support in cross-functional meetings.

  • Partners with stakeholders (e.g., GCDS, Study Statistical Programmers, Data Management) to define user-defined specifications, align priorities, and deliver solutions.

  • Builds cross-functional buy-in and influences decisions related to tools, standards, and timelines.

  • May interact with external vendors and ensures alignment with internal standards.

Communication & Decision-Making

  • Communicates effectively with stakeholders across multiple functions and organizational levels.

  • Resolves conflicts and escalates risks appropriately while maintaining project momentum.

Basic Qualifications

  • PhD with 5+ years

OR

  • MS with 8+ years,

OR

  • BS with 10+ years of relevant experience in statistical programming or related field.

Preferred Qualifications

  • MS with 8+ years,

OR

  • BS with 10+ years of relevant experience in statistical programming or related field.

  • Significant experience in life sciences, including clinical trials, analysis, and regulatory reporting.

  • Demonstrated experience leading projects and/or teams.

  • Knowledge of internal Gilead Analysis and Reporting macros is not required but desired.

Skills & Competencies

  • Advanced expertise in statistical programming and tool development (SAS Macro required).

  • Strong understanding of clinical trial design and reporting process, as well as regulatory requirements.

  • Strong problem-solving, negotiation, and decision-making skills.

  • Excellent verbal and written communication and interpersonal skills are required.


The salary range for this position is:

Other US Locations: $177,905.00 - $230,230.00.


Bay Area: $195,670.00 - $253,220.00.


Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.
For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.


For jobs in the United States:

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