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Junior Statistical Programmer Analyst _Permanent Role_(CANADA)

ClinChoice
Remote, CAN
Full-time
Entry · 0+ years experience
Remote
CAD 60-70 yearly / year
Discovered 3 weeks ago
SASRSAS Macro

Full Job Posting

Responsibilities

  • Programming for Clinical Trials
  • 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.
  • Electronic Submissions
  • 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.
  • Quality and Validation
  • 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.
  • Standards and Guidelines
  • 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.

Qualification & Experience

  • 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.
  • Open Date: 9/29/2026
  • Close Date: 11/23/2026
  • ClinChoice Canada Inc. is proud to be an equal opportunity employer, valuing and respecting diversity. We are committed to inclusive, barrier-free recruitment and selection processes. We will accommodate the needs of qualified applicants under the Human Rights Code and the Accessibility for Ontarians Disabilities Act, in all aspects of the hiring process, upon request by calling + 1 (647)724-5709 x 301.
  • We thank all applicants for their interest; however, only those being considered for an interview will be contacted. In accordance with Federal Personal Information Protection and Electronic Documents Act ("PIPEDA") , personal information is collected under the authority of the Act and will only be used for candidate selection.
  • #LI-TT1 #LI-Remote #LI-Junior #Permanent
  • The base salary pay range represents the anticipated low and high range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.
  • Canada Pay Range
  • $60 — $70 CAD

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