Senior Clinical & Statistical Programmer

Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families. Umoja Biopharma – Your Body. Your Hope. Your Cure. POSITION SUMMARY The Senior Clinical & Statistical Programmer will perform clinical and statistical programming activities across Umoja’s clinical development programs, including the development, validation, and quality control of analysis datasets, tables, listings, and figures (TLFs). As an experienced individual contributor, this role will provide hands-on SAS programming expertise, review work produced by CROs and external partners, troubleshoot complex data and programming issues, and support clinical trial execution and regulatory submission readiness. This position will collaborate closely with Biostatistics, Clinical Data Management, Clinical Operations, Medical, Safety, and Regulatory Affairs to ensure high-quality, timely deliverables that meet CDISC standards, regulatory requirements, and internal quality standards. This role will ideally be based out of our Seattle, WA location and work onsite at least 2 days per week. We are open to remote candidates within the U.S. for the right candidate. CORE ACCOUNTABILITIES Specific responsibilities include: Perform hands-on clinical and statistical programming activities across the clinical trial lifecycle, ensuring timely and high-quality deliverables. Develop, validate, and QC SDTM and ADaM datasets, specifications, tables, listings, and figures (TLFs) in accordance with CDISC standards. Provide hands-on SAS programming support for safety, efficacy, exploratory, ad hoc, and publication analyses. Review clinical trial protocols, statistical analysis plans (SAPs), CRFs, and data specifications to ensure programming requirements are appropriately addressed. Perform quality control and validation of programming deliverables and identify and resolve programming or data-related issues. Review programming deliverables produced by CROs, contractors, and external collaborators for quality, accuracy, and compliance with established standards. Support the preparation of regulatory submission deliverables, including SDTM and ADaM datasets, TLFs, define.xml, reviewer guides, and associated documentation. Support programming activities associated with INDs, BLAs, and other regulatory submissions or requests. Collaborate closely with Biostatistics, Clinical Data Management, Clinical Operations, Medical, Safety, and Regulatory Affairs to address data and programming needs. Contribute to the development and maintenance of reusable programs, macros, programming standards, SOPs, and other tools that improve programming quality and efficiency. Support internal and external audits, inspections, and regulatory inquiries related to clinical and statistical programming deliverables. The successful candidate will have: BS in Biostatistics, Statistics, Computer Science, or a closely related field; MS preferred. Minimum of 5 years of relevant clinical and statistical programming experience within the pharmaceutical, biotechnology, or CRO environment, with experience in hands-on programming, development and validation of clinical trial deliverables, study execution, regulatory submission support, and programming standards and processes. Strong knowledge of statistical programming principles, advanced SAS programming expertise, experience preparing regulatory submission packages, and strong knowledge of CDISC standards. <li data-leveltext="" data-font="Symbol" data-listid="5" data-list-defn-props="{"335552541":1,"335559685":720,"335559991":360,"469769226":"Symbol","469769242":[8226],"469777803":"left","469777804":"","469777