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Clinical Statistical Programmer Jobs in Seattle, WA

Systimmune

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond ... The Statistical Programmer will support statistical programming activities for clinical trials ...

SystImmune, Inc

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond ... The Statistical Programmer will support statistical programming activities for clinical trials ...

Systimmune

Director, Clinical Data Management

Redmond, WA · On-site

$190K - $250K/yr

The successful candidate will collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Clinical Development, Pharmacovigilance, Regulatory Affairs, and external partners ...

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 ...

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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 Jul 26, 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 July 2026, with employment types broken down into 100% Full Time. Highlights an 88% In-person, and 12% Remote job distribution, with an average salary of $128,249 per year, or $61.7 per hour.
Statistical Programmer

Statistical Programmer

Systimmune

Redmond, WA • On-site

$80K - $100K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 18 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.
The Statistical Programmer will support statistical programming activities for clinical trials, including generating SDTM/ADaM datasets, tables, figures, and listings (TFLs). This role is ideal for someone early in their career who is eager to learn and grow in a fast-paced biotech environment with exposure to end-to-end clinical development.
This position is full-time onsite at our Redmond, WA location and we will be moving to our new location in Bothell, WA fall 2026. We will consider candidates for our Princeton, NJ location on a case by case basis. 
Responsibilities
  • Collaborate with biostatisticians and cross-functional study team members to deliver statistical analysis and reporting outputs in line with project timelines.
  • Review study documents including statistical analysis plans (SAPs), CRFs, database specifications, and data transfer specifications.
  • Create and/or review SDTM/ADaM mapping specifications and annotated CRFs (aCRFs).
  • Generate and/or validate SDTM and ADaM datasets, including associated Define.xml and reviewer’s guides.
  • Develop and validate tables, figures, and listings (TFLs) to support clinical study analyses, regulatory submissions, conferences, and publications.
  • Assess the quality, integrity, and consistency of analysis datasets, including cross-study analyses where applicable.
  • Develop SAS programs and macros to automate dataset generation and reporting deliverables.
  • Contribute to process improvements and enhancements of the statistical programming environment.
  • Participate in study team meetings and representing statistical programming in cross-functional discussions.
  • Apply knowledge of clinical trial design, CDISC standards, and regulatory requirements while producing analysis datasets and outputs in compliance with SOPs and industry standards.
 
Qualifications
  • Master’s degree or higher in Biostatistics, Statistics, Mathematics, or a related scientific discipline, with 0–2 years of experience in statistical programming within the pharmaceutical/biotech industry or a CRO.
  • Proficiency in SAS programming, preferably with experience in a clinical trial environment.
  • Working knowledge of CDISC standards (SDTM and ADaM).
  • Hands-on experience in developing and validating SDTM and ADaM datasets, as well as statistical outputs (tables, figures, and listings).
  • Prior experience or exposure to oncology studies is preferred.
  • Strong analytical, problem-solving, and organizational skills.
  • Effective communication and interpersonal skills, with the ability to work collaboratively in cross-functional teams.

Compensation and Benefits:
The expected base salary range for this position is $80,000 - $100,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s level 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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