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Full Time Statistical Programmer Jobs (NOW HIRING)

SystImmune, Inc

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

The Statistical Programmer will support statistical programming activities for clinical trials ... This position is full-time onsite at our Redmond, WA location and we will be moving to our new ...

New

Systimmune

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

The Statistical Programmer will support statistical programming activities for clinical trials ... This position is full-time onsite at our Redmond, WA location and we will be moving to our new ...

New

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Full Time Statistical Programmer information

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How much do full time statistical programmer jobs pay per year?

As of Jul 14, 2026, the average yearly pay for full time statistical programmer in the United States is $147,292.00, according to ZipRecruiter salary data. Most workers in this role earn between $125,000.00 and $160,000.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Statistical Programmer vs Clinical Data Analyst?

AspectFull Time Statistical ProgrammerClinical Data Analyst
Required CredentialsBachelor's or Master’s in Statistics, Biostatistics, or related field; programming skills in SAS, R, or PythonBachelor's or Master’s in Statistics, Data Science, or related; strong analytical and programming skills
Work EnvironmentPharmaceutical or biotech companies, CROs, clinical research settingsHealthcare organizations, research institutions, pharmaceutical companies
Employer & Industry UsageCommonly employed in clinical trials to generate statistical reportsFocuses on data interpretation, reporting, and supporting clinical decision-making

The main difference is that Full Time Statistical Programmers primarily develop and validate statistical programs for clinical trials, while Clinical Data Analysts focus on analyzing and interpreting clinical data to support research and decision-making. Both roles require strong programming skills and work in similar environments, but their core responsibilities differ.

What cities are hiring for Full Time Statistical Programmer jobs? Cities with the most Full Time Statistical Programmer job openings:
What are the most commonly searched types of Statistical Programmer jobs? The most popular types of Statistical Programmer jobs are:
Full Time Statistical Programmer jobs near you
Statistical Programmer

Statistical Programmer

SystImmune, Inc

Redmond, WA • On-site

$80K - $100K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago

New

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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