Senior Statistical Analyst II

Bilinguallink; Kitchener; On-site; CAD 90,000 - 130,000; Full time

Job summary

Bilinguallink is seeking an experienced SAS programmer to lead complex programming efforts within pharmaceutical or CRO environments in Canada. The role focuses on developing ADaM and TFL analyses, creating macros, and guiding junior team members.

You will serve as the project lead programmer, manage timelines, and act as the primary programming contact for clients, ensuring adherence to ICH-GCP and regulatory standards.

Qualifications

• Bachelor's degree or above in Statistics, Mathematics, Computer Science, or related field.
• 5+ 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.

Responsibilities

• Develop and validate complex 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 and managing timelines.
• Communicate with clients as the key programming contact and deliver outputs.

Skills

SAS programming

Project leadership

Clinical trials knowledge

Regulatory knowledge

Communication skills

Education

Bachelor's degree in Statistics/Math/CS

Tools

SAS software

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.
• 5+ 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 SAS software.