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Clinical Statistical Programmer Jobs in Seattle, WA

Systimmune

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project Managers, Clinical Trial Managers, CRAs, Clinical Pharmacologists, Biomarker/Bioinformatics ...

SystImmune, Inc

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project Managers, Clinical Trial Managers, CRAs, Clinical Pharmacologists, Biomarker/Bioinformatics ...

Systimmune

Biostatistician - Bilingual Mandarin

Bothell, WA · On-site

$80K - $140K/yr

Experience with statistical programming such as SAS, R, Python. * Experience with CDISC and CDASH standards. * Strong knowledge and experience in clinical trial design and data analysis, with ability ...

Karius

Clinical Sales Manager (Seattle)

Seattle, WA · Remote

$118K - $177K/yr

The Clinical Sales Manager is responsible for the sales efforts of Karius in a defined regional ... Our test is the result of some incredible work done by our scientists, statisticians, engineers ...

Karius

Clinical Sales Manager (Seattle)

Seattle, WA · On-site

The Clinical Sales Manager is responsible for the sales efforts of Karius in a defined regional ... Our test is the result of some incredible work done by our scientists, statisticians, engineers ...

Karius

Clinical Sales Manager (Seattle)

Seattle, WA · On-site +1

The Clinical Sales Manager is responsible for the sales efforts of Karius in a defined regional ... Our test is the result of some incredible work done by our scientists, statisticians, engineers ...

Natera

Associate Clinical Oncology Specialist

Tacoma, WA · On-site

$110K - $130K/yr

The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory ... engineers and many other professionals from world-class institutions, who care deeply for our work ...

Natera

Clinical Oncology Specialist, Breast

Seattle, WA · On-site

$195K - $225K/yr

The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory ... engineers and many other professionals from world-class institutions, who care deeply for our work ...

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Showing results 21-40

All JobsClinical Statistical Programmer JobsClinical Statistical Programmer Jobs in Seattle, WA

Clinical Statistical Programmer information

See Seattle, WA salary details

$18

$61

$102

How much do clinical statistical programmer jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical statistical programmer in Seattle, WA is $61.66, according to ZipRecruiter salary data. Most workers in this role earn between $39.13 and $92.74 per hour, depending on experience, location, and employer.

What are some common challenges faced by clinical statistical programmers when working with clinical trial data?

Clinical Statistical Programmers often encounter challenges such as handling large and complex datasets, ensuring data integrity, and adhering to strict regulatory guidelines (like CDISC standards). Collaborating closely with biostatisticians, data managers, and clinical teams is essential to resolve data discrepancies and meet tight project deadlines. Staying updated on evolving regulatory requirements and software tools is also vital to maintain high-quality deliverables in a fast-paced environment.

What are the key skills and qualifications needed to thrive as a clinical statistical programmer, and why are they important?

To thrive as a Clinical Statistical Programmer, you need strong proficiency in statistical programming languages (such as SAS or R), a background in statistics or life sciences, and familiarity with clinical trial processes. Experience with CDISC standards (SDTM, ADaM), regulatory submission requirements, and version control systems is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring data quality. These skills ensure the accurate analysis and reporting of clinical data, which is critical for regulatory compliance and successful clinical trial outcomes.

What does a clinical statistical programmer do?

A Clinical Statistical Programmer is responsible for managing and analyzing clinical trial data using statistical software, such as SAS or R. Their primary tasks include creating datasets, programming statistical analyses, and generating tables, listings, and figures for clinical study reports. They work closely with biostatisticians and clinical research teams to ensure data accuracy and regulatory compliance. Their work is essential for supporting submissions to regulatory agencies and for making data-driven decisions in clinical research.

What does a clinical statistical programmer do?

The job duties of a clinical statistical programmer involve collecting data, performing statistical analysis, and analyzing data sets according to the needs of their employer or client. Your responsibilities in this career may involve using SAS programming to create and analyze data sets during clinical trials or other clinical experiments and studies. You may also be involved in performing data integration for reports following clinical research or statistical analysis for quality control (QC).

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Clinical Statistical Programmer jobs near you
Infographic showing various Clinical Statistical Programmer job openings in Seattle, WA as of August 2026, with employment types broken down into 3% As Needed, 73% Full Time, 16% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $128,247 per year, or $61.7 per hour.

Associate Director / Director, Biostatistics

Immunome, Inc.

Bothell, WA • On-site

$235K - $263K/yr

Full-time

Re-posted 14 days ago

Job description

Company Overview
Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been accepted by the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-1617, a clinical-stage solid tumor ADC; and IM-3050, a clinical-stage FAP-targeted radioligand therapy. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets.
Position Overview
The Associate Director / Director, Biostatistics provides statistical support to clinical studies, including the design, analyses, and interpretation of clinical trials. This position collaborates closely with cross-functional teams and provides scientifically rigorous statistical expertise on projects and protocols in support of clinical development and for publication and presentation.
Responsibilities
  • Apply rigorous statistical expertise to study design, statistical analysis plans, interpretation of results, project development plans, and regulatory issues.
  • Provide strategic statistical input into clinical development plans and study-level decision-making, anticipating downstream regulatory and data implications to inform study design and overall development strategy.
  • Plan, deliver, and communicate statistical analyses and scientific reports, including clinical trial and exploratory analyses, and support publications and scientific presentations.
  • Own the timeliness and quality of study- and submission-level statistical deliverables on assigned projects. For outsourced studies, manage vendors and monitor their performance and adherence to project timelines.
  • Ensure all study- and project-level statistical activities are conducted in compliance with relevant regulatory requirements (e.g., FDA regulations).
  • Contribute to interactions with regulatory authorities (e.g., FDA, EMA), including statistical input for regulatory meetings, responses to health authority questions, and preparation for advisory committee meetings.
  • Collaborate with internal partners (e.g., clinical development, clinical data management, statistical programming) to provide statistical support and help identify and resolve data issues.
  • Develop and lead initiatives in process improvement, training, and standard development.
  • Support ad hoc analyses and develop and validate programs for data analysis, reporting, and visualization.

Qualifications
  • PhD or Master's in Biostatistics, Statistics, or a related field.
  • A minimum of 6 years (with a PhD) or 8 years (with a Master's) of biostatistics experience supporting clinical trials in the pharmaceutical, biotech, or CRO industry, or equivalent.
  • A minimum of 2 years of leadership or people-management experience is preferred.

Knowledge and Skills
  • Prior oncology clinical trial experience, including familiarity with standard response criteria (e.g., RECIST 1.1), oncology endpoints (e.g., overall survival, progression-free survival, objective response rate), and associated statistical methodology (e.g., survival/time-to-event analysis, group sequential and adaptive designs).
  • Experience supporting regulatory submissions (e.g., NDA, BLA) is a strong plus.
  • Experience managing CROs and external statistical vendors, including oversight of outsourced statistical deliverables, is a plus.
  • Proficiency in statistical programming languages (e.g., SAS, R); experience using simulation to support trial design is a plus.
  • Knowledge of CDISC data standards (SDTM and ADaM).
  • Knowledge of drug submission requirements and relevant ICH and FDA/EMA guidelines, including the ICH E9(R1) estimand framework.
  • Strong verbal and written communication skills, including the ability to convey complex statistical concepts to cross-functional, non-statistical audiences.
  • Strong problem-solving skills and the ability to work both independently and collaboratively in a fast-paced environment.
  • Strong attention to detail and a proven ability to manage multiple competing priorities.

Washington State Pay Range - Associate Director: $200,850 - $227,316
Washington State Pay Range - Director: $235,000 - $263,700
Washington State Pay Range
$200,850-$263,700 USD
E/E/O
Immunome, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
E-Verify
Immunome, Inc. is a participant in E-Verify. Please review the following notices: E-Verify Participation Poster | Right to Work Poster (English) | Right to Work Poster (Spanish).

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