Statistical Programmer Analyst (SAS)

TL;DR

Statistical Programmer Analyst (SAS): Developing and validating statistical programs for clinical trial data analysis with an accent on generating Tables, Listings, and Figures (TLFs). Focus on ensuring compliance with CDISC standards and supporting regulatory submissions in a collaborative CRO environment.

Location: Must be based in Ontario, Canada (Hybrid: 2 days a week in office).

Salary: $50–$70 CAD per hour.

Company

hirify.global is a global full-service CRO committed to professional growth and a quality-driven one-team culture.

What you will do

• Develop and validate statistical programs using SAS for TLFs.
• Perform data manipulation, analysis, and visualization using R and SAS.
• Collaborate with Biostatisticians and Data Management teams on study deliverables.
• Ensure compliance with regulatory standards and company SOPs.
• Conduct quality control and validation of programming outputs.
• Support submission activities and documentation.

Requirements

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

Nice to have

• Hands-on experience with R programming in a clinical trial environment.
• Experience working in an FSP model or with global pharmaceutical clients.
• Exposure to FDA/EMA submission activities.

Culture & Benefits

• Commitment to professional growth and development.
• Quality-driven and inclusive team culture.
• Supportive environment for clinical research professionals.