Junior Statistical Programmer Analyst – Permanent Role

ClinChoice

. Support the development and validation of datasets, tables, figures, and listings for clinical trials.

Posted 11/4/2026full-timeRemote • CanadaJunior💰 CA$60,000 - CA$70,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates proficiency in statistical programming using SAS and R, with a solid understanding of CDISC standards, including SDTM and ADaM. Capable of supporting clinical trial data development and validation while ensuring adherence to quality standards and timelines.

Highest-signal resume keywords

SAS ProgrammingR ProgrammingCDISC StandardsSDTM DevelopmentADaM Development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical ProgrammingData ValidationProgramming SpecificationsClinical Trial DocumentationProgramming MacrosData IntegrationQuality ChecksAd Hoc AnalysesDataset DevelopmentProgramming Utilities

Soft Skills

Attention to DetailTeam CollaborationTask ManagementLearning Agility

Industry Keywords

Clinical TrialsPharmaceutical IndustryBiotechnologyCROClinical Research

About the role

Key responsibilities & impact

Support the development and validation of datasets, tables, figures, and listings for clinical trials.
Perform programming activities using SAS and/or R under appropriate guidance and review.
Assist with processing and integrating data from internal and external sources.
Support ad hoc analyses and programming activities for clinical development and other Research & Development functions.
Assist with the development, review, and maintenance of programming specifications and documentation.
Contribute to the development and review of SDTM and ADaM datasets and specifications.
Support the preparation and review of Define-XML and other clinical trial documentation.
Work closely with Senior Statistical Programmers, Biostatisticians, Data Managers, and other cross-functional team members.
Support the programming and validation of CDISC-compliant datasets and deliverables for regulatory submissions.
Assist with the preparation of supporting documentation for electronic submissions.
Ensure programming outputs follow applicable standards, specifications, and quality requirements.
Perform programming validation and quality checks according to established procedures.
Identify, document, and resolve programming issues in collaboration with senior team members.
Ensure assigned deliverables are completed accurately and within agreed timelines.
Follow departmental programming standards, working instructions, and applicable industry guidelines.
Develop knowledge of CDISC standards, including SDTM and ADaM.
Assist in maintaining and improving programming macros, utilities, and reusable functions.

Requirements

What you’ll need

Bachelor's or Master's degree in Computer Science, Statistics, Mathematics, Engineering, Life Sciences, or a related discipline.
0–2 years of experience in statistical programming, preferably within the pharmaceutical, biotechnology, CRO, or clinical research industry.
Basic to intermediate knowledge of SAS and/or R.
Familiarity with SAS programming and SAS Macro language is preferred.
Basic understanding of clinical trial data and the drug development process.
Knowledge or exposure to CDISC standards, SDTM, and ADaM is preferred.
Familiarity with clinical trial datasets, tables, figures, and listings is an advantage.
Strong attention to detail and commitment to data quality.
Ability to work effectively in a team environment and learn from senior team members.
Ability to manage assigned tasks and meet project timelines.

Benefits

Comp & perks

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