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
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.
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
Categories
- Data & Analytics
- Healthcare
- Science & Research
- Technology
- Consulting
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