1482# Principal Statistical Programmer Consultant(Oncology) - Remote in US

Bachelor's or Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field. 8–12+ years of statistical programming experience in pharma/biotech or CRO. Expert-level proficiency in SAS. Strong understanding of CDISC SDTM and ADaM standards. Significant experience supporting oncology clinical trials. Experience supporting regulatory submissions. Excellent communication and collaboration skills.

Lead programming activities for oncology clinical trials. Develop, validate, and maintain SDTM and ADaM datasets. Oversee production of Tables, Listings, and Figures (TLFs). Provide SAS programming expertise for complex data derivations. Ensure quality and traceability of programming deliverables. Act as programming lead for assigned studies, managing timelines. Collaborate with Biostatistics, Data Management, and Regulatory Affairs. Coordinate with CROs and external vendors. Support integrated analyses (ISS/ISE). Prepare submission-ready programming outputs and documentation. Ensure programming meets regulatory requirements. Contribute to responses for regulatory queries.