Senior Statistical Analyst I

Bilinguallink; Richmond Hill; On-site; CAD 90,000 - 120,000; Full time

Job summary

Bilinguallink in Richmond Hill, Ontario, seeks an experienced SAS programmer to develop and validate complex analysis datasets (ADaM) and TFLs, write specifications, and lead projects.

You will mentor juniors, coordinate with global clients, ensure adherence to ICH-GCP and CDISC, and archive deliverables per SOPs.

Qualifications

• Bachelor’s degree in Statistics, Mathematics, Computer Science, or related field.
• 3+ years of SAS programming experience in pharmaceutical or CRO environments.
• Strong knowledge of clinical trials, statistical methods, and regulatory requirements.
• Proven experience leading programming projects and mentoring team members.
• Excellent communication skills and experience working with global teams and clients.
• Proficient in Microsoft Office and SAS software.

Responsibilities

• Develop and validate complex analysis datasets (ADaM) and TFLs using SAS.
• Write and review programming specifications and supporting documentation.
• Create standard macros and tools to improve efficiency.
• Serve as project lead programmer, assigning tasks and managing timelines.
• Communicate with clients as the key programming contact and manage feedback.
• Conduct SAS code reviews and ensure quality standards.
• Archive all programming deliverables per SOPs.
• Mentor team members and support their development.
• Ensure compliance with ICH-GCP, CDISC standards, and SOPs.

Skills

SAS programming

Leading programming projects

Communication skills

Mentoring team members

Global collaboration

Education

Bachelor’s degree in Statistics, Mathematics, Computer Science, or related field

Tools

SAS software

Microsoft Office

Job description

Key Responsibilities

• Develop and validate complex analysis datasets (ADaM) and TFLs using SAS.


• Write and review programming specifications and supporting documentation.


• Create standard macros and tools to improve efficiency.


• Serve as a project lead programmer, assigning tasks, managing timelines, and providing technical guidance to junior team members.


• Communicate with clients as the key programming contact, including delivering outputs and managing feedback.


• Conduct SAS code review, track issues, and ensure quality standards are met.


• Archive all programming deliverables and documentation per SOPs.


• Mentor team members and support their technical and professional development.


• Ensure compliance with ICH-GCP, CDISC standards, and company SOPs.

Requirements

• Bachelor’s degree or above in Statistics, Mathematics, Computer Science, or related field.


• 3+ years of SAS programming experience in pharmaceutical or CRO environments.


• Strong knowledge of clinical trials, statistical methods, and regulatory requirements.


• Proven experience leading programming projects and mentoring team members.


• Excellent communication skills and experience working with global teams and clients.


• Proficient in Microsoft Office and SAS software.