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Senior Statistical Programmer Analyst Jobs (NOW HIRING)

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

The Statistical Programmer will support statistical programming activities for clinical trials ... Review study documents including statistical analysis plans (SAPs), CRFs, database specifications ...

Statistical Programmer

Redmond, WA · On-site

$80 - $100/hr

The Statistical Programmer will support statistical programming activities for clinical trials ... Review study documents including statistical analysis plans (SAPs), CRFs, database specifications ...

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

The Statistical Programmer will support statistical programming activities for clinical trials ... Review study documents including statistical analysis plans (SAPs), CRFs, database specifications ...

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

The Statistical Programmer will support statistical programming activities for clinical trials ... Review study documents including statistical analysis plans (SAPs), CRFs, database specifications ...

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

The Statistical Programmer will support statistical programming activities for clinical trials ... Review study documents including statistical analysis plans (SAPs), CRFs, database specifications ...

The role of the Senior Statistical Programmer is to perform statistical programming activities for ... Create data definition tables for analysis data sets for all assigned studies and integrated ...

The (Senior) Principal Programmer works within BeOne's Statistical Programming group to manage and ... Write, test, and validate SAS programs to produce analysis datasets, tables, listings, graphs, and ...

The (Senior) Principal Programmer works within BeOne's Statistical Programming group to manage and ... Analytical Thinking/Data Analysis * Financial Excellence * Communicates with Clarity Salary Range ...

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W2 Expectation: Sr. level 5+ yrs exp. Medical affairs, publication support, mainly use clinical ... Generate analysis datasets according to CDISC standard and SAP. * Implement analysis methods ...

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Senior Statistical Programmer Analyst information

See salary details

$82.5K

$128.3K

$167.5K

How much do senior statistical programmer analyst jobs pay per year?

As of Sep 7, 2026, the average yearly pay for senior statistical programmer analyst in the United States is $128,293.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,000.00 and $148,000.00 per year, depending on experience, location, and employer.

What does a senior statistical programmer analyst do?

A Senior Statistical Programmer Analyst is responsible for designing, developing, and validating statistical programs that analyze clinical trial or research data. They work closely with biostatisticians and data managers to ensure data accuracy, integrity, and compliance with regulatory standards. Their work includes creating tables, listings, and figures (TLFs), developing analysis datasets, and automating data processes. Senior Statistical Programmer Analysts often mentor junior programmers and play a key role in quality control and project delivery within pharmaceutical, biotechnology, or clinical research organizations.

How does a senior statistical programmer analyst typically collaborate with cross-functional teams in clinical research projects?

As a Senior Statistical Programmer Analyst, you will regularly collaborate with biostatisticians, data managers, clinical research associates, and project managers. Your main responsibility is to translate statistical analysis plans into programming code (often using SAS or R), ensuring datasets and outputs meet regulatory standards. You’ll participate in team meetings to clarify study requirements, address data or programming issues, and ensure timelines are met. Strong communication and documentation skills are essential, as you often serve as a bridge between technical and non-technical team members.

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

To thrive as a Senior Statistical Programmer Analyst, you need advanced programming skills in SAS or R, a strong background in statistics, and a relevant degree such as in mathematics, statistics, or computer science. Experience with clinical trial data, CDISC standards (SDTM, ADaM), and regulatory submission processes, along with certifications like SAS Certified Professional, are highly valued. Exceptional problem-solving abilities, attention to detail, and effective communication enable you to manage complex datasets and collaborate with cross-functional teams. These combined skills ensure accurate data analysis, regulatory compliance, and successful delivery of biostatistical projects in the pharmaceutical or clinical research industry.
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Infographic showing various Senior Statistical Programmer Analyst job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 6% Part Time, and 5% Contract. Highlights an 82% Physical, 7% Hybrid, and 11% Remote job distribution, with an average salary of $128,293 per year, or $61.7 per hour.

Statistical Programmer

SystImmune, Inc

Redmond, WA • On-site

$80K - $100K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 12 hours 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.