Job Title

**Must be eligible to work in Canada without restrictions****Must have extensive lead experience****Must have extensive Oncology experience**We are seeking a highly skilled Senior Statistical Programmer. This is a lead role and will be responsible for the end-to-end programming and validation of clinical trial datasets, tables, listings, and figures (TLFs) in compliance with regulatory standards. The ideal candidate will have extensive experience supporting oncology clinical trials (Phases IIII) and working closely with Biostatisticians, Data Management, and Clinical teams to deliver high-quality outputs for regulatory submissions.QualificationsEducation: Masters degree in Statistics requiredRequired SkillsProficiency in SAS programming (Base, Macro, SQL).Strong knowledge of CDISC SDTM and ADaM implementation guidelines.5+ years of statistical programming experience in the pharmaceutical/biotech/CRO industry.Experience with regulatory submissions (FDA, EMA, PMDA) preferred.Lead and Client facing experience preferredPreferred SkillsExcellent problem-solving skills, attention to detail, and ability to manage multiple priorities.Strong communication skills and ability to work in a collaborative, fast-paced environment.