Statistical Programming Specialist in Clinical Trials Support
Location
markham, york region
Job Type
Full-time
Category
IT & Technology
Posted
June 01, 2026
Become a vital contributor as a Statistical Programming Specialist in clinical trials. Develop and validate datasets, ensuring data integrity and compliance in a dynamic research environment.
You'll be responsible for programming SDTM and ADaM datasets and crafting SAS output for clinical study reports. Collaborate with Data Managers to enhance data quality during trials and support the overall integrity of the research process. Ideal candidates will have a strong background in statistics and bioinformatics.
Key Responsibilities:
• Develop specifications for statistical datasets
• Validate datasets and perform compliance checks
• Generate SAS programming for trial statistics
• Conduct data integrity checks and rectifications
• Document programming processes thoroughly
Requirements:
• Master’s or Ph.D. required in relevant discipline
• SAS certification (Base/Advanced) is a must
• Experience in statis...
You'll be responsible for programming SDTM and ADaM datasets and crafting SAS output for clinical study reports. Collaborate with Data Managers to enhance data quality during trials and support the overall integrity of the research process. Ideal candidates will have a strong background in statistics and bioinformatics.
Key Responsibilities:
• Develop specifications for statistical datasets
• Validate datasets and perform compliance checks
• Generate SAS programming for trial statistics
• Conduct data integrity checks and rectifications
• Document programming processes thoroughly
Requirements:
• Master’s or Ph.D. required in relevant discipline
• SAS certification (Base/Advanced) is a must
• Experience in statis...