Senior Statistical Programmer (Granby)

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 Canada. Key responsibilities Statistical programming - Participate in all statistical programming activities across the full clinical data lifecycle, from raw data to submission - Develop SAS programs for SDTM conversions, ADaM analysis datasets, and study TFLs based on SAPs, shells, and CDISC or client-specific instructions - Develop core programs for validation, conversion, and maintenance of clinical data dataset structures - Create programming specification documents for all data types including SDTM, ADaM, and derived data - Review and verify all conversions and programming outputs against customer requirements Submissions & standards - Prepare clinical data for regulatory submissions using CDISC or customized standards - Prepare submission documents including Reviewer's Guides and Define.xml - Contribute to the development of best practices and implementation guides Project management & mentorship - May be responsible for project or program-level management including timelines, scope, budget, and resourcing - Train, mentor, and share knowledge with other members of the statistical programming team - Interact directly with clients at the project or program level as needed Compliance - Follow applicable Standard Operating Procedures (SOPs) for all statistical programming activities Education - Bachelor's degree in Statistics, Computer Science, Life Sciences, or a related discipline Experience - 6+ 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 progression - Solid TFL programming experience - Experience programming to CDISC standards (SDTM, ADaM) and preparing regulatory submission documents - Experience working across FSP and in-house environments, or across multiple client engagements Skills - Robust SAS programming skills across the full end-to-end clinical programming workflow - Excellent client-facing communication skills — written and verbal - High attention to detail with the ability to review and validate complex programming outputs - Adaptable and comfortable operating in fast-changing environments across different client standards and expectations Apply on Kit Job: kitjob.ca/job/2o12i3