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Added 13 days ago
T
Clinical Project Manager-Neurology
Tigermed
Canada
- Full-time
Added 1 month ago
T
CRA/SCRA-Canada
Tigermed
Canada
- Full-time
Added 6 months ago
T
Senior Statistical Analyst I
Tigermed
Canada
- Full-time
Added 6 months ago
T
Senior Statistical Analyst II
Tigermed
Canada
- Full-time

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Tigermed

Senior Statistical Analyst II

Canada

Full-time

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Job details

Job type: Full-time
Experience: 5+ years of SAS programming experience in pharmaceutical or CRO environments.
Posting language: English
Posted: Apr 14, 2026

Original 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.

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More about this job

Responsibilities

The Senior Statistical Analyst II will develop and validate complex analysis datasets and TFLs using SAS, while also serving as a project lead programmer. Responsibilities include writing programming specifications, mentoring team members, and ensuring compliance with regulatory standards.

Requirements

Candidates should have a bachelor's degree or higher in a relevant field and at least 5 years of SAS programming experience in pharmaceutical or CRO environments. Strong knowledge of clinical trials and experience in leading programming projects are also required.

Skills

SAS Programming
Statistical Analysis
Clinical Trials
Regulatory Requirements
Project Management
Mentoring
Communication
Data Validation
Quality Assurance
Technical Guidance
Documentation
ADaM
TFLs
Macros
ICH-GCP
CDISC Standards

Visa sponsorship

Not detected in the job text

Keywords

SAS
Statistical Analysis
ADaM
TFLs
Clinical Trials
Pharmaceutical
CRO
Regulatory Requirements
ICH-GCP
CDISC
Programming Specifications
Macros
Data Validation
Quality Assurance
Project Management
Mentoring
Documentation

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Open jobs in Canada

Clinical Project Manager-Neurology

CRA/SCRA-Canada

Senior Statistical Analyst I

Senior Statistical Analyst II