Statistical Programmer

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 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, along with a robust preclinical pipeline in the discover and IND‑enabling stages.

This position is full‑time onsite at our Redmond, WA location and will move to our new Bothell, WA location in fall 2026. Candidates for the Princeton, NJ location may be considered 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 represent 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 of 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 exceed the requirements of the role.

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.

SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.