Statistical Programmer Analyst I/II -Permanent Role- Hybrid (2 days a week)

ClinChoiceOntario, Canada, ON
CA$50 - CA$70Hybrid

About The Position

ClinChoice is a global full-service CRO committed to professional growth and a quality-driven “one-team” culture. We are seeking a Statistical Programmer Analyst I/II to join our in-house team and support projects across a diverse client portfolio, including pharmaceutical, biotechnology, medical device, and consumer health companies of varying sizes. We are seeking an experienced Statistical Programmer Analyst I/II with strong expertise in SAS programming to support clinical trial data analysis and reporting. The ideal candidate will have hands-on experience in developing, validating, and maintaining statistical outputs using R/SAS, along with a solid understanding of clinical data standards.

Requirements

  • Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, or a related field
  • 3+ years of experience in statistical programming within the pharmaceutical/biotech industry
  • Good understanding of R packages.
  • Good understanding of CDISC standards (SDTM, ADaM)
  • Strong knowledge of clinical trial data and regulatory requirements

Nice To Haves

  • Hands-on experience with R programming in a clinical trial environment is a plus.
  • Experience working in an FSP model or with global pharmaceutical clients
  • Exposure to submission activities (e.g., FDA/EMA)
  • Familiarity with SAS alongside R is a plus
  • Strong problem-solving and communication skills

Responsibilities

  • Develop, validate, and maintain statistical programs using SAS for the generation of Tables, Listings, and Figures (TLFs)
  • Perform data manipulation, analysis, and visualization using R/SAS and relevant packages
  • Collaborate with Biostatisticians and Data Management teams to support clinical study deliverables
  • Ensure compliance with regulatory standards and company SOPs
  • Conduct quality control (QC) and validation of programming outputs
  • Support submission activities and documentation as required
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