Programming Engineer

Redmond, WA

About the position

Located in Redmond WA, SystImmune Inc. is a bio-pharmaceutical company focused on the treatment of cancer through developing novel therapeutic bi-specific, and tri-specific antibodies, as well as antibody-drug conjugates (ADC's). Our objective is to create biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor and/or to activate the immune system to attack the tumor. We are a group of highly experienced immuno-oncology scientists utilizing several technology platforms to develop world class advanced antibody-based drug therapies.

We have an immediate opening for a Programming Engineer to join our organization. The ideal candidate is highly energetic and motivated in supporting the growth of the organization as it continues create more data.

Major Responsibilities

  • Maintain and develop new features for our LIMS.
  • Design, develop, and support ETL components to move data from lab instruments into the data warehouse.
  • Develop analysis pipelines from scientific data.
  • Gather requirements from scientific staff and translate that into code.
  • Work closely with scientific staff to identify short\long term goals for application development
  • Provide support and fix bugs as needed.
  • Manage database servers.
  • Provide application support to staff.
  • Experience in using SAS-Base, MACRO, STAT, GRAPH
  • Write SAS programs to generate derived analysis datasets
  • Provide programming input to CRF, SAP, analysis file specifications, and tables, figures, and listings (TFLs) shells.
  • Support the clinical research and clinical trials programming
  • Other duties as assigned.


  • Full-stack web development.
  • Experience in data modeling and data warehouse architecture.
  • Expertise in SQL.
  • Experience with agile development and continuous integration pipelines.
  • Ability to work with others and communicate technology issues to non—technical staff.
  • Professional software development experience, preferably with JavaScript and Python
  • Ability to learn new programming skills as needed
  • knowledge with CDISC/SDTM requirements for compliant datasets, programs, and validation process
  • Understanding FDA guidelines.

Preferred Qualifications

  • Experience working in a biotech, pharmaceutical, research, or health institute setting.
  • Infrastructure automation / scripting experience (Bash, Terraform, PowerShell, Python).
  • Knowledge of data analysis tools such as Tableau, JMP, SAS, R, Matlab, Pandas, etc.
  • Experience with regulatory requirements (21 CFR Part 11).
  • Experience in design and perform quality checks on analysis datasets, tables, listings, figures (TFL), and written reports to support clinical trial results using SAS
  • Experience in create and review annotated CRF to STDM datasets


  • Bachelor's Degree in Computer Science or Equivalent experience will be considered
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