Senior Statistical Programmer Analyst

ClinChoice

. Lead and support statistical programming activities for clinical trials .

Posted 11/4/2026full-timeRemote • CanadaSenior💰 CA$80,000 - CA$95,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in statistical programming for clinical trials, with strong proficiency in SAS and R, and a solid understanding of CDISC standards and the drug development process. Capable of delivering high-quality programming outputs while effectively collaborating with cross-functional teams and managing external vendors.

Highest-signal resume keywords

Statistical ProgrammingSAS ProgrammingR ProgrammingCDISC ComplianceData Integration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical ProgrammingSASRSAS Macro LanguageData IntegrationCDISC StandardsDerived DatasetsStatistical Analysis PlansCase Report FormsDefine Packages

Soft Skills

Strong Communication SkillsCollaborationTechnical Guidance

Industry Keywords

Pharmaceutical IndustryClinical TrialsDrug Development ProcessExternal VendorsCROs

About the role

Key responsibilities & impact

Lead and support statistical programming activities for clinical trials
Program and validate derived datasets, tables, figures, and listings
Process data from external sources
Perform ad hoc exploratory analyses for publications and support other Research and Development functions
Oversee programming work and deliverables from CROs
Contribute to the design, implementation, and review of Case Report Forms, Data Transfer Specifications, Statistical Analysis Plans, SDTM/ADaM specifications, and Define packages
Program and validate CDISC-compliant deliveries for electronic submissions
Support creation of submission documentation
Ensure programming deliverables are timely and high quality
Help manage internal contractors and external vendors
Participate in developing departmental working instructions and guidelines
Help create enhanced functions, macros, and utilities
Provide technical guidance to other programmers and collaborate with cross-functional teams and external vendors

Requirements

What you’ll need

Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline
BS with more than 5 or MS with 3 years of experience in statistical programming (SAS, R) in the pharmaceutical industry
Working knowledge of SAS and its various components
Knowledge of R programming in clinical trials
Familiarity with the drug development process
Strong SAS and SAS Macro language skills
Strong knowledge of industry standards
Ability to work on data integrations (ISS and ISE)
Strong oral and written communication skills
Ability to communicate details of the analysis to other team members with less technical experience

Benefits

Comp & perks

Equal opportunity employer
Inclusive, barrier-free recruitment and selection processes
Accommodation for qualified applicants under the Human Rights Code and the Accessibility for Ontarians Disabilities Act