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Associate Director Statistical Programming Jobs in El Sobrante, CA

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Associate Director Statistical Programming information

See El Sobrante, CA salary details

$165.5K

$302K

$370.9K

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

As of Aug 20, 2026, the average yearly pay for associate director statistical programming in El Sobrante, CA is $302,015.00, according to ZipRecruiter salary data. Most workers in this role earn between $280,800.00 and $347,700.00 per year, depending on experience, location, and employer.

What does an associate director 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.

What are the key skills and qualifications needed to thrive as an associate director statistical programming?

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 does an associate director 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 cities near El Sobrante, CA are hiring for Associate Director Statistical Programming jobs?

Cities near El Sobrante, CA with the most Associate Director Statistical Programming job openings:

Associate Director Statistical Programming jobs near you
Infographic showing various Associate Director Statistical Programming job openings in El Sobrante, CA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, and 40% Hybrid job distribution, with an average salary of $302,015 per year, or $145.2 per hour.

Sr. Director, Biostatistics

ALX Oncology Inc.

South San Francisco, CA • On-site

$240K/yr

Full-time

Retirement

Re-posted 29 days ago

Job description

The Senior Director, Biostatistics provides strategic statistical leadership across ALX Oncology's clinical development portfolio, partnering cross-functionally to design, execute, analyze, and interpret clinical studies that support regulatory submissions and advance innovative oncology therapies. This role drives statistical strategy, oversees outsourced biostatistics activities, and collaborates closely with Clinical Development, Translational Medicine, Biomarker Sciences, Regulatory Affairs, Data Management, Statistical Programming, Clinical Operations, and external partners.
Preference will be given to candidates who can regularly work onsite Mondays and Tuesdays as part of the company's hybrid work model.
Key Responsibilities include:
  • Lead the Biostatistics function by developing and executing strategies that support ALX Oncology's clinical development portfolio, providing strategic leadership across oncology programs from early development through registration and lifecycle management.
  • Direct statistical strategy for registrational clinical trials, including innovative adaptive and biomarker-driven study designs, and provide expertise in study design, endpoint selection, estimands, multiplicity control, interim analyses, missing data, sensitivity analyses, and benefit-risk assessments.
  • Oversee the development, review, and approval of key statistical deliverables, including protocols, statistical analysis plans (SAPs), clinical study reports (CSRs), regulatory briefing documents, publications, and scientific presentations.
  • Drive adaptive design evaluations and statistical simulations to support study design, operating characteristics, power calculations, and informed decision-making throughout clinical development.
  • Provide statistical leadership for global regulatory interactions, health authority submissions, companion diagnostic (CDx) and biomarker-driven development programs, partnering closely with cross-functional teams to ensure compliance with applicable regulatory requirements and industry standards.
  • Oversee CROs, external statistical vendors, budgets, and outsourced Biostatistics activities, ensuring high-quality deliverables, effective governance, and operational excellence.
  • Provide technical leadership and mentorship across the Biometrics organization, fostering collaboration, innovation, and the adoption of statistical best practices.
  • Contribute to business development, due diligence, portfolio strategy, and other strategic initiatives as needed.
  • Contribute to a culture that reflects ALX's values by acting with integrity, accountability, transparency, and respect. Build strong, collaborative relationships through active engagement with colleagues, including regular onsite participation consistent with the company's hybrid work model.

Not sure if you are qualified for this position? We know that skills and experience can show up in different ways and we welcome resumes from a broad range of applicants. You are encouraged to apply even if you do not meet each of the preferred qualifications.
Preferred Qualifications include:
  • Bachelor's degree in Statistics, Biostatistics, Mathematics, Life Sciences, Computer Science, or a related quantitative discipline, or an equivalent combination of education and directly relevant work experience. Advanced degree (MS, PhD, or equivalent) in a quantitative discipline is strongly preferred.
  • Approximately 12+ years of progressive Biostatistics experience within biotechnology, pharmaceutical, or CRO environments, including Phase I-III oncology clinical studies, with demonstrated success leading statistical strategy for registrational clinical trials, partnering across cross-functional teams, and supporting global regulatory submissions.
  • Experience with companion diagnostic (CDx) co-development, biomarker-driven development strategies, and interactions with global health authorities.
  • Deep expertise in biostatistical principles, oncology clinical trial methodology, GCP, applicable regulatory requirements, and industry best practices including study design, adaptive clinical trial methodologies, survival analysis, estimands, multiplicity adjustment, missing data methodology, interim analyses, and companion diagnostic statistical approaches.
  • Proficiency with statistical programming and analysis software, including SAS and R. Experience with adaptive design and simulation software (e.g., EAST, ADDPLAN, or equivalent).
  • Strategic, collaborative leader with excellent communication, organizational, and relationship-building skills, capable of influencing cross-functional teams and external partners.
  • Demonstrated ability to prioritize competing demands, solve complex problems, build scalable processes, and adapt to evolving business priorities while contributing beyond functional boundaries in a fast-paced, resource-constrained environment.

Compensation
The salary range for this position at our South San Francisco, CA corporate office is $240,000 - $280,000. Additional factors such as academic credentials and relevant experience will influence the actual salary offered. In addition to a competitive market-based salary, ALX Oncology offers the opportunity to participate in stock programs, a performance-based bonus, and a comprehensive benefits package including 401K. Additional information can be found here: https://alxoncology.com/careers/
About ALX Oncology
ALX Oncology (Nasdaq: ALXO) is a clinical-stage biotechnology company advancing a pipeline of novel therapies designed to treat cancer and extend patients' lives. ALX Oncology's lead therapeutic candidate, evorpacept, has demonstrated potential to serve as a cornerstone therapy upon which the future of immuno-oncology can be built. Evorpacept is currently being evaluated across multiple ongoing clinical trials in a wide range of cancer indications. ALX Oncology's second pipeline candidate, ALX2004, is a novel EGFR-targeted antibody-drug conjugate with a differentiated mechanism of action. A Phase 1, dose-escalation trial of ALX2004 is ongoing in patients with EGFR-expressing solid tumors. More information is available at www.alxoncology.com and on LinkedIn @ALX Oncology.
Information for Recruitment Agencies
Please note that ALX Oncology does not accept unsolicited resumes or candidate information from recruitment agencies, including blinded or anonymized resumes, and will not be responsible for any fees associated with unsolicited submissions. Do not contact hiring managers or other ALX Oncology employees directly. Recruiting activities are managed through our Human Resources team.

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