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Director Statistical Programming Jobs in California

Reporting to the Sr. Director, Biostatistics and Data Management, this individual will; * Provide ... SOP), Statistical Analysis Systems (SAS) Programming The anticipated base pay range for this ...

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As a Director of Biostatistics at Gilead, you will... Requirements: * Provide Statistical ... Works collaboratively with Statistical Programming, Biostatistics, Clinical Research, Clinical Data ...

As a Director of Biostatistics at Gilead, you will... Requirements: * Provide Statistical ... Works collaboratively with Statistical Programming, Biostatistics, Clinical Research, Clinical Data ...

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Director Statistical Programming information

See California salary details

$151.5K

$276.5K

$339.5K

How much do director statistical programming jobs pay per year?

As of Jul 13, 2026, the average yearly pay for 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 a Director of Statistical Programming, and why are they important?

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

What Is the Job of a Director Statistical Programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

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

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.

What does a Director of Statistical Programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.
What are the most commonly searched types of Statistical Programming jobs in California? The most popular types of Statistical Programming jobs in California are:
What are popular job titles related to Director Statistical Programming jobs in California? For Director Statistical Programming jobs in California, the most frequently searched job titles are:
What job categories do people searching Director Statistical Programming jobs in California look for? The top searched job categories for Director Statistical Programming jobs in California are:
What cities in California are hiring for Director Statistical Programming jobs? Cities in California with the most Director Statistical Programming job openings:
Infographic showing various Director Statistical Programming job openings in California as of July 2026, with employment types broken down into 91% Full Time, and 9% Part Time. Highlights an 80% In-person, 6% Hybrid, and 14% Remote job distribution, with an average salary of $276,479 per year, or $132.9 per hour.
Associate Director, Biostatistics

Associate Director, Biostatistics

Corcept Therapeutics

Redwood City, CA • On-site

$183K - $269K/yr

Full-time, Contractor

Posted 20 days ago


Job description

For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases.
Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today.
Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com.
The Associate Director of Biostatistics will be responsible for leading the execution of statistical components of Corcept Development programs. This position will manage external statisticians and statistical programmers.
This is a hybrid role typically requiring on-site presence at least 3 days per week.
Responsibilities:
  • Partner with Clinical Development, Regulatory, Manufacturing, and Commercial organizations on the design and execution of clinical trials in the Corcept portfolio
  • Oversee execution of the statistical components of clinical studies by CROs and independent contractors. Manage on-time and quality delivery of CRO-generated analyses results
  • Partner with Statistical Programming in generation of statistical analyses for internal and external presentations, and validation statistical analyses results generated by CROs
  • Partner with Statistical Programming in the evaluation of CDISC electronic data packages for completeness, regulatory standards compliance, and submission readiness
  • Stay current with regulatory requirements for statistical methods of analyses and scientific developments in statistical methods for clinical trials
  • Consult internal audit team in assessing regulatory compliance of CROs with respect to statistical SOPs
  • Participate in standards governance and development of Corcept Biostatistical SOPs

Preferred Skills, Qualifications, and Technical Proficiencies:
  • Knowledge of global regulatory guidance on statistical methods for analyses of clinical data, and global submission requirements
  • Proficiency with statistical programming in SAS. Familiarity with SAS/GRAPH, SAS/MACRO, and R
  • Demonstrated ability to apply complex statistical methods, conduct and interpret the results

Preferred Education and Experience:
  • D. in Statistics, Biostatistics, or Mathematics
  • 5+ years of experience in clinical trial development
  • Demonstrated ability for project management of projects in clinical development
  • Experience managing delivery of statistical projects by CROs

The pay range that the Company reasonably expects to pay for this headquarters-based position is $183,500 - $269,800; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.
Applicants must be currently authorized to work in the United States on a full-time basis.
For information on how Corcept collects, uses, discloses, protects, and otherwise processes personal information and an explanation of the rights and choices available to you with respect to your personal information, please refer to our Privacy Notice link.
Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs.
Please visit our website at: https://www.corcept.com/
Corcept is an Equal Opportunity Employer
Corcept will not conduct interviews via text message or messaging platforms and will not ask you to download anything as part of your interview. Though we use third-party tools to help with advertising our jobs, please be vigilant in checking that the communication is in fact coming from Corcept.