Posted last month
Senior Statistical Analyst I
@ Tigermed
Canada
SIGNALS
Overview
Tigermed is hiring a Senior Statistical Analyst I to develop and validate ADaM datasets and TFLs in SAS for clinical trials. The role leads programming projects, mentors junior programmers, and serves as the key client programming contact.
Responsibilities:
- Develop and validate ADaM datasets and TFLs using SAS
- Lead programming projects and mentor junior team members
- Serve as key client programming contact and manage feedback
- Conduct SAS code review and ensure quality standards
- Ensure ICH-GCP, CDISC, and SOP compliance
Requirements summary:
- Bachelor's degree or above in a quantitative or computing field
- 3+ years of SAS programming in pharma or CRO
- Strong clinical trial and regulatory knowledge
- Experience leading programming projects and mentoring
- Excellent communication with global teams and clients
Tools & skills
Source and dates
Source type not verified · apify-linkedin
- Employer posting date
- 2026-10-07
- 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 | Data & analytics |
| Experience | 3+ years |
| 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.
- 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.
Journal
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