Programming Engineer

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.

Qualifications

• 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

Education

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