Senior Statistical Programmer - SAS & CDISC Lead

Cytel; Toronto; On-site; CAD 80,000 - 100,000; Full time

Job summary

A leading clinical data solutions provider in Toronto is seeking an experienced professional to provide technical leadership in SAS programs and applications. The ideal candidate should possess a master’s degree in biostatistics or a related field with over 8 years of experience within the pharmaceutical industry. Responsibilities include ensuring compliance with FDA regulations, performing quality control on SAS code, and conducting technical briefings. Excellent communication skills and adaptability are essential for this role.

Qualifications

• 8+ years of experience in the pharmaceutical industry for MS holders.
• 10+ years of experience in the pharmaceutical industry for BS holders.

Responsibilities

• Provide technical leadership in SAS programs and applications.
• Ensure compliance with company SOPs and FDA regulations.
• Perform quality control checks of SAS code.
• Review and maintain study documents.
• Conduct briefings and participate in technical meetings.

Skills

Expert in SAS language, procedures, and options

R programming experience

Excellent communication skills

Adaptability and flexibility

Education

MS in biostatistics or related field

BS in biostatistics or related field

Job description

A leading clinical data solutions provider in Toronto is seeking an experienced professional to provide technical leadership in SAS programs and applications. The ideal candidate should possess a master’s degree in biostatistics or a related field with over 8 years of experience within the pharmaceutical industry. Responsibilities include ensuring compliance with FDA regulations, performing quality control on SAS code, and conducting technical briefings. Excellent communication skills and adaptability are essential for this role.