Statistical Programmer Analyst I/II -Permanent Role-Hybrid @ Ontario Canada

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.

Job Summary: 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.

Key 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

Required Skills & Qualifications:

• 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
• Hands-on experience with R programming in a clinical trial environment is a plus.
• Good understanding of R packages.
• Good understanding of CDISC standards (SDTM, ADaM)
• Strong knowledge of clinical trial data and regulatory requirements

Preferred Qualifications:

• Experience working in an FSP model or with global pharmaceutical clients
• <span style="font-family: tahoma, arial, helvetica,