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

📋 Description

• Develop and maintain SAS programs for Tables, Listings, and Figures
• Analyze data and visualize results using R/SAS
• Collaborate with Biostatisticians and Data Management
• Ensure regulatory compliance and SOP adherence
• QC and validation of programming outputs
• Support submission activities and documentation

🎯 Requirements

• Bachelor’s or Master’s in Statistics, Biostatistics, CS, or related field
• 3+ years statistical programming in pharma/biotech
• Hands-on R programming in clinical trials
• Strong knowledge of CDISC standards (SDTM, ADaM)
• Familiarity with FDA/EMA submission activities
• Strong problem-solving and communication skills

🎁 Benefits

• Hybrid work arrangement with 2 days/week in Ontario, Canada
• Equal opportunity employer; diversity and inclusion
• Accommodations under AODA and Human Rights Code; contact +1 647-724-5709 x301