Senior Statistical Programmer

We are seeking a well-rounded Statistical Programmer to join a fast-moving clinical programming team supporting multiple clients and study types. This is a client-facing role requiring strong communication skills alongside deep technical expertise. The ideal candidate is adaptable, independently driven, and comfortable shifting between FSP and in-house environments — often with different standards and expectations client to client.**Candidates must be based in U.S. OR Canada - No sponsorship or Corps at this time***Key responsibilitiesStatistical programmingParticipate in all statistical programming activities across the full clinical data lifecycle, from raw data to submissionDevelop SAS programs for SDTM conversions, ADaM analysis datasets, and study TFLs based on SAPs, shells, and CDISC or client-specific instructionsDevelop core programs for validation, conversion, and maintenance of clinical data dataset structuresCreate programming specification documents for all data types including SDTM, ADaM, and derived dataReview and verify all conversions and programming outputs against customer requirementsSubmissions & standardsPrepare clinical data for regulatory submissions using CDISC or customized standardsPrepare submission documents including Reviewer's Guides and Define.xmlContribute to the development of best practices and implementation guidesProject management & mentorshipMay be responsible for project or program-level management including timelines, scope, budget, and resourcingTrain, mentor, and share knowledge with other members of the statistical programming teamInteract directly with clients at the project or program level as neededComplianceFollow applicable Standard Operating Procedures (SOPs) for all statistical programming activitiesEducationBachelors or Master's degree in Statistics, Biostatistics, Computer Science, Mathematics, or a related disciplineExperience5+ years of experience as a statistical programmer working on clinical trials; candidates with 4–5 years may be considered with a strong track record of rapid career progressionSolid TFL programming experienceExperience programming to CDISC standards (SDTM, ADaM) and preparing regulatory submission documentsExperience working across FSP and in-house environments, or across multiple client engagementsTherapeutic Area: Oncology (primary)SkillsStrong SAS programming skills across the full end-to-end clinical programming workflowExcellent client-facing communication skills — written and verbalHigh attention to detail with the ability to review and validate complex programming outputsAdaptable and comfortable operating in fast-changing environments across different client standards and expectations