Statistical Programmer (Onsite) - SAS, CDISC, Oncology

SystImmune; Redmond (WA); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Medical/dental/vision coverage

401(k) with company match

Paid time off 15 days

Job summary

SystImmune in Redmond, WA seeks a statistical programmer for onsite work with a plan to move to Bothell, WA in fall 2026. Princeton, NJ may be considered case-by-case.

You will develop SDTM/ADaM datasets, create TFLs, and support regulatory submissions using SAS in a clinical trial setting. Master’s in Biostatistics or related field and 0–2 years of experience are required, with emphasis on CDISC standards and cross-functional collaboration in oncology studies.

Qualifications

• Master’s degree or higher in Biostatistics, Statistics, Mathematics, or related field, with 0–2 years of experience in statistical programming.
• Proficiency in SAS programming, preferably in a clinical trial environment.
• Working knowledge of CDISC SDTM/ADaM standards.
• Hands-on experience in developing/validating SDTM/ADaM datasets and outputs.
• Experience in oncology studies is preferred.
• Strong analytical, problem-solving, and organizational skills.
• Effective communication and collaboration in cross-functional teams.

Responsibilities

• Collaborate with biostatisticians and study team members to deliver statistical analyses and reports.
• Review SAPs, CRFs, database specs, and data transfer specs.
• Create/review SDTM/ADaM mappings and aCRFs.
• Generate SDTM/ADaM datasets and Define.xml, reviewer’s guides.
• Develop tables, figures, and listings to support analyses and regulatory submissions.
• Assess quality and consistency of analysis datasets across studies.
• Develop SAS programs/macros to automate dataset generation and reporting.

Skills

SAS programming

CDISC SDTM/ADaM

Analytical skills

Cross-functional collaboration

Education

Master’s degree in Biostatistics or related field

Tools

SAS software

Job description

SystImmune in Redmond, WA seeks a statistical programmer for onsite work with a plan to move to Bothell, WA in fall 2026. Princeton, NJ may be considered case-by-case.

You will develop SDTM/ADaM datasets, create TFLs, and support regulatory submissions using SAS in a clinical trial setting. Master’s in Biostatistics or related field and 0–2 years of experience are required, with emphasis on CDISC standards and cross-functional collaboration in oncology studies.