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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 10, 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, Statistical Programming

Associate Director, Statistical Programming

Annexon Biosciences

San Francisco, CA • On-site

$194K - $216K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 20 days ago

Job description

Company:
At Annexon Biosciences we are a biopharmaceutical company advancing a late-stage clinical platform of novel therapies for people living with devastating classical complement-mediated neuroinflammatory diseases of the body, brain, and eye. Our novel scientific approach targets upstream C1q to block the classical complement inflammatory cascade before it starts, and its therapeutic candidates are designed to provide meaningful benefits across multiple autoimmune, neurodegenerative and ophthalmic diseases. With proof-of concept data in Guillain-Barré syndrome, Huntington's disease and geographic atrophy, we are rigorously advancing our mid-to late-stage clinical trials to bring new potential treatments to patients as quickly as possible. At Annexon, you'll be part of a team committed to making an impact together.
For more information on Annexon and our pipeline, check out our site Annexon Biosciences & Annexon Pipeline. We trade on Nasdaq under the ticker symbol ANNX and are headquartered in Brisbane, CA.
We're seeking exceptional talent from all backgrounds to fuel our growth. At Annexon, we're building a diverse, equitable, and inclusive workplace. We value unique perspectives and unconventional paths. If you're the best candidate for the job, even if you don't perfectly fit the traditional mold, we encourage you to apply. Learn more about our commitment to diversity, equity, inclusion, and our company culture!
Position:
Reporting to the Head of Statistical Programming, this individual independently operates and oversees the development and delivery of statistical programming solutions for all Annexon clinical trials and regulatory submissions. A highly visible and collaborative role, the Associate Director of Statistical Programming partners cross-functionally to advance medicines to our patients.
Responsibilities include:
  • Manage timelines and provide sponsor oversight for statistical programming deliverables outsourced to biometrics vendors (CROs) with full E2E traceability.
  • Serve as lead statistical programmer on one or more clinical studies.
  • Conducts gap analysis and risk assessments for global submissions such as BLA/MAA etc.
  • Reviews SAP, TFL shells, eCRFs etc.
  • Maintain complete and auditable documentation for all statistical programming activities.
  • Develop and/or verify CDISC SDTM/ADaM specifications, datasets and eCRT submission packages such as define.xml, reviewer's guide's etc.
  • Support supplemental/ad hoc/post hoc requests for submissions, publications and manuscripts.
  • Provide guidance to project/study teams.
  • Participate cross-functionally with key partners to advance Annexon products.
  • Contribute to and participate in the development and maintenance of a positive team-focused company culture.

Education, Experience, and Skills:
Required:
  • MS with 8+ years of experience or BS with 10+ years of experience in the pharmaceutical or biotechnology industry in a Statistical Programming leadership capacity.
  • In-depth knowledge of CDISC standards.
  • Prior FDA and EMA submissions experience.
  • Technical expertise and knowledge of experimental design and analyses using statistical software such as SAS etc.
  • Understanding of GCP, ICH, 21 CFR Part 11 standards.
  • Work in dynamic, demanding and collaborative environment.

Preferred:
  • Ability to communicate with clarity and influence including explaining complex quantitative issues in simple terms.
  • Solid understanding of Regulatory (FDA/EMA/ICH) guidance with the ability to interpret and apply in real-time drug development setting.
  • Understanding of regulatory submission and approval process.
  • Ability to effectively collaborate and influence throughout multiple levels of the organization.
  • Strategic and creative drug-development mindset/approach.
  • Ability to balance appropriate levels of structure/process with efficiency and simplicity.
  • Awareness of external industry landscape with respect to best practices and emerging topics.

Salary Range: $194,000 - $216,000
Location: Annexon Biosciences is located in Brisbane, California and preference is given to candidates in the San Francisco Bay Area.
Benefits:
  • A stimulating and rewarding workplace includes flexible work schedules, remote opportunities and the ability to achieve a work-life balance.
  • Shuttle service from BART, CalTrain and the Ferry.
  • Annexon offers a competitive base salary and equity participation, employee stock purchase plan, as well as a comprehensive health benefit package that includes medical, dental, vision, 401(k), flexible spending plans, and other benefits.

Annexon Biosciences is an Equal Opportunity Employer, and we prohibit discrimination or harassment of any kind. We are committed to fostering an environment where ALL people are welcome and supported. We cultivate a culture of inclusion for all employees that respects their individual strengths, views, and experiences. We believe that our differences enable us to be a better team - one that makes better decisions, drives innovation, and delivers better business results. Creativity and innovation flourish in an environment of openness, inclusion, and mutual respect.

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