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Director Statistical Programming Jobs in Seattle, WA

Chewy

Associate Director, Data Science

Bellevue, WA · On-site

Your Opportunity Chewy is seeking an innovative and strategic Associate Director, Data Science to ... D.) in Data Science, Computer Science, Statistics, Engineering, or a related quantitative field ...

Chewy

Associate Director, Data Science

Bellevue, WA

Your Opportunity Chewy is seeking an innovative and strategic Associate Director, Data Science to ... D.) in Data Science, Computer Science, Statistics, Engineering, or a related quantitative field ...

Microsoft

Director, People Analytics

Redmond, WA · On-site

The People Analytics Director for Microsoft Commercial Business will serve as the strategic ... Statistics, Mathematics, Analytics, Data Science, Engineering, Computer Science, Business ...

YMCA

Teen Director

Tacoma, WA · On-site

$23.70 - $26.38/hr

... programming options around those interests. * Positive attitude and previous experience with teens ... Compile program statistics. Monitor and evaluate the effectiveness of and participation in the ...

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Director Statistical Programming information

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$174.8K

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How much do director statistical programming jobs pay per year?

As of May 31, 2026, the average yearly pay for director statistical programming in Seattle, WA is $318,994.00, according to ZipRecruiter salary data. Most workers in this role earn between $296,600.00 and $367,200.00 per year, depending on experience, location, and employer.

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.

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.

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.
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Director Statistical Programming jobs near you
Infographic showing various Director Statistical Programming job openings in Seattle, WA as of May 2026, with employment types broken down into 9% As Needed, 78% Full Time, 9% Part Time, 3% Contract, and 1% Summer. Highlights an 74% Physical, 8% Hybrid, and 18% Remote job distribution, with an average salary of $318,994 per year, or $153.4 per hour.
Sr. Manager/Associate Director, Statistical Programming

Sr. Manager/Associate Director, Statistical Programming

SystImmune, Inc

Redmond, WA • On-site

$150K - $200K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 22 days ago

Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is seeking a Senior Manager or Associate Director of Statistical Programming to lead statistical programming activities across complex clinical development programs. This role oversees high-quality, on-time delivery of datasets, TLGs, and regulatory submissions, manages and develops programming teams and vendors, and serves as the programming lead on key studies. The position partners closely with biostatistics and cross-functional teams to support study design, regulatory readiness, and continuous improvement of programming standards and processes, and can be based in Sugar Land, TX, Princeton, NJ, or Redmond, WA.
This is a bilingual role in Chinese and English.
Responsibilities
  • Responsible for statistical programming activities within a therapeutic project or equivalent
  • Lead, manage, develop and support statistical programming team
  • Manage critical deadlines, demonstrate ability to problem solving, and ensure quality statistical programming deliverables will be completed within designated timeframe.
  • Serve as project leader on studies or tasks of greater complexity
  • Attend multi-disciplinary team meetings, representing the statistical programming function.
  • Create or review and approve programming plans at study and project level.
  • Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plan, SAPs, etc.)
  • Provide programming leadership for preparation of datasets and TLGs (NDA/BLA) to FDA, EMA, or other worldwide regulatory agencies
  • Develop software systems to generate displays of clinical study data as tables, listings, and graphs for electronic submission to regulatory agencies
  • Assist statisticians by suggesting algorithms to address novel analysis requests
  • Develop software validation procedures and test plans, as necessary.
  • Create and document archives of software, outputs, and analysis files.
  • Contribute to the creation and maintenance of department SOPs related to clinical data analysis.
  • Review draft clinical reports, journal articles, slide presentations, and other documents to assure that results are reported accurately.
  • Oversee work of internal contract programmers and external vendors.
  • Provide time and resource estimates for project planning.

Requirements
  • BSc or MS (in a numerate discipline preferably in Statistics, Computer Science, or Mathematics)
  • Preferably at least 10 years of experience in biostatistics or statistical programming activities in the Pharmaceutical/Biotechnology industry in clinical development
  • At least 5 years of experience as a statistical programming team leader or manager
  • Fluency in English and Chinese
  • Strong knowledge of relevant regulatory (FDA, NMPA, EMA, PMDA etc.) and data submission guidelines
  • Strong understanding of drug development, including knowledge of interfaces and interdependencies with other functions
  • Consistent experience as a lead statistical programmer on several concurrent NDA projects
  • Strong knowledge of the relevant therapeutic areas and CDISC standards
  • Self-directed, technically strong, and a recognized leader maintaining a strategic prospective with regard to statistical programming processes, management of statistical programmers and customer management
  • Strong project management skills

Compensation and Benefits:
The expected base salary range for this position is $150,000 - $200,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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