Posted 27 days ago
Senior Statistical Analyst II
@ Tigermed
Canada
SIGNALS
Overview
Tigermed is hiring a Senior Statistical Analyst II to lead SAS programming on clinical trial projects. The role builds ADaM datasets and TFLs, leads a programming team, and serves as the client's key programming contact. The posting requires 5+ years of SAS experience in pharma or CRO settings and a Bachelor's degree or higher.
Responsibilities:
- Develop and validate ADaM datasets and TFLs using SAS
- Lead programming projects, assign tasks and manage timelines
- Serve as key programming contact for clients
- Conduct SAS code review and ensure quality standards
- Mentor junior team members
Requirements summary:
- Bachelor's degree or above in Statistics, Mathematics, Computer Science or related field
- 5+ years of SAS programming in pharma or CRO
- Strong knowledge of clinical trials and regulatory requirements
- Proven experience leading programming projects
- Excellent communication with global teams and clients
Tools & skills
Source and dates
Source type not verified · apify-linkedin
- Employer posting date
- 2026-10-15
- First seen by our source
- 2026-11-11
- Source record updated
- 2026-11-11
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Senior |
| Department | Software development |
| Experience | 5+ years |
| Manages people | Yes |
| Hours per week | 40 (estimated) |
| Work setting | Office |
| Position | Mostly sitting |
| Physical demands | physical low · computer high |
| Languages | English |
| Education | Bachelor’s degree (required) |
| Fields of study | Statistics, Mathematics, Computer Science |
Summary and details written by AI from the posting; the employer’s posting is the authority.
Tigermed
| Field | Value |
|---|---|
| Open jobs on Jobsy | 3 |
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.
Journal
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