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Clinical Statistical Programmer Jobs in Bellevue, WA

SystImmune, Inc.

Statistical Programmer

Redmond, WA · On-site

$80 - $100/hr

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, 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

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

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 ...

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Clinical Statistical Programmer information

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How much do clinical statistical programmer jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical statistical programmer in Bellevue, WA is $60.81, according to ZipRecruiter salary data. Most workers in this role earn between $38.56 and $91.44 per hour, depending on experience, location, and employer.

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).

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 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.
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Clinical Statistical Programmer jobs near you
Infographic showing various Clinical Statistical Programmer job openings in Bellevue, WA as of August 2026, with employment types broken down into 2% As Needed, 71% Full Time, 20% Part Time, and 7% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $127,191 per year, or $61.1 per hour.

Clinical Statistical Programmer

Collabera Digital

Seattle, WA • On-site

$150K - $160K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 14 days ago

Key responsibilities

  • Provide hands-on expertise in ADaM dataset structure and TLF development.

  • Review and validate AI-generated ADaM/TLF outputs against CDISC standards and FDA submission requirements.

  • Support the preparation and review of FDA submission packages, including Define.xml and related documentation.

Job description

About Ascendion
Ascendion is a full-service digital engineering solutions company. We make and manage software platforms and products that power growth and deliver captivating experiences to consumers and employees. Our engineering, cloud, data, experience design, and talent solution capabilities accelerate transformation and impact for enterprise clients. Headquartered in New Jersey, our workforce of 6,000+ Ascenders delivers solutions from around the globe. Ascendion is built differently to engineer the next.
Ascendion | Engineering to elevate life
We have a culture built on opportunity, inclusion, and a spirit of partnership. Come, change the world with us:
  • Build the coolest tech for world's leading brands
  • Solve complex problems - and learn new skills
  • Experience the power of transforming digital engineering for Fortune 500 clients
  • Master your craft with leading training programs and hands-on experience

Experience a community of change makers!
Join a culture of high-performing innovators with endless ideas and a passion for tech. Our culture is the fabric of our company, and it is what makes us unique and diverse. The way we share ideas, learning, experiences, successes, and joy allows everyone to be their best at Ascendion.
About the Role:
Now Hiring: ADaM/TLF & FDA Submission Expert
Location:Hybrid as needed 2 days/week in Seattle, WA
Ascendion is hiring anADaM/TLF & FDA Submission Expertto support a confidential Fortune 500 technology client developing next-generation AI solutions for clinical trial data and regulatory submissions.
This is a unique opportunity for an experienced clinical data professional with deep expertise inADaM, TLFs, CDISC standards, and FDA submissionsto help validate AI-generated clinical trial outputs. You'll work alongside engineering and clinical teams to ensure AI-generated deliverables meet real-world regulatory and submission standards.
Key Responsibilities
  • Provide hands-on expertise in ADaM dataset structureandTLF (Tables, Listings & Figures)development.
  • Review and validate AI-generated ADaM/TLF outputs againstCDISC standardsandFDA submission requirements.
  • Support the preparation and review ofFDA submission packages, includingDefine.xmland associated documentation.
  • Identify compliance gaps, inconsistencies, and submission risks while providing actionable feedback.
  • Partner with engineering and clinical teams to translate regulatory requirements into AI development guidance.
  • Ensure submission-ready data meets quality, compliance, and regulatory expectations.

Required Qualifications
  • Proven hands-on experience building and/or submittingADaM datasetsandTLF packagesfor clinical trial submissions.
  • Strong knowledge ofCDISC ADaM,SDTM, and FDA submission standards.
  • Experience supportingFDA submission packagesfor clinical trials.
  • Strong analytical, problem-solving, and written communication skills.
  • Ability to review technical outputs and identify regulatory compliance issues.

Preferred Qualifications
  • Experience working withAI-assisted clinical dataor AI-generated outputs.
  • Experience inGxP-regulatedenvironments.
  • Background in pharmaceutical, biotechnology, or CRO organizations.
  • Experience collaborating with cross-functional teams, including biostatistics, clinical programming, regulatory affairs, and engineering.

Why Join?
  • Work on cutting-edgeAI solutions transforming clinical trial data and regulatory submissions.
  • Collaborate with a leading Fortune 500 technology company.
  • Flexiblepart-timeengagement with a highly specialized, high-impact project.
  • Opportunity to shape the future of AI in clinical research and regulatory compliance.

If you have hands-on expertise inADaM, TLFs, FDA submissions, CDISC, Define.xmlwe'd love to hear from you!
Salary Range: The salary for this position is between $150,000 - $160,000 annually. Factors which may affect pay within this range may include geography/market, skills, education, experience and other qualifications of the successful candidate.
Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: [medical insurance] [dental insurance] [vision insurance] [401(k) retirement plan] [long-term disability insurance] [short-term disability insurance] [personal days accrued each calendar year. The Paid time off benefits meet the paid sick and safe time laws that pertains to the City/ State] [12-15 days of paid vacation time] [6-8 weeks of paid parental leave after a year of service] [9 paid holidays and 2 floating holidays per calendar year] [Ascendion Learning Management System] [Tuition Reimbursement Program]
Want to change the world? Let us know.
Tell us about your experiences, education, and ambitions. Bring your knowledge, unique viewpoint, and creativity to the table. Let's talk!
Preferred Skills
ADaM
  • TLF
  • ADaM dataset
  • FDA Submisson
  • Define.XML

Job details
Job ID 332874
Role Clinical Statistical Programmer
Location Seattle, Washington, US
Job type Direct Hire
Recruiter Divya
Email divy.tandel@ascendion.com
About Ascendion
Ascendion is a full-service digital engineering solutions company. We make and manage software platforms and products that power growth and deliver captivating experiences to consumers and employees.
Our engineering, cloud, data, experience design, and talent solution capabilities accelerate transformation and impact for enterprise clients. Headquartered in New Jersey, our workforce of 6,000+ Ascenders delivers solutions from around the globe. Ascendion is built differently to engineer the next.

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