Posted 9 days ago
Senior Statistical Programmer
@ Warman O'Brien
Canada
Overview
Warman O'Brien is hiring a Senior Statistical Programmer for a small CRO growing its Biometrics group. The role leads complex clinical trial programming projects, including SDTM and ADaM datasets and regulatory submissions. The posting states it is full-time and remote or hybrid.
Responsibilities:
- Lead statistical programming for complex clinical trial projects
- Create and validate SDTM and ADaM dataset specifications
- Program and validate datasets with data integrity checks
- Mentor junior programmers and lead project teams
- Contribute to regulatory submissions and client bid defences
Requirements summary:
- Master's or PhD in Statistics, Biostatistics, Epidemiology or Computer Science
- 6+ years of clinical trial statistical programming experience
- Experience with clinical trial data, SDTM/ADaM and regulatory submissions
Tools & skills
Source and dates
Source type not verified · apify-linkedin
- Employer posting date
- 2026-11-01
- First seen by our source
- 2026-11-10
- Source record updated
- 2026-11-10
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 | 6+ years |
| Hours per week | 40 (estimated) |
| Work setting | Home, Office |
| Position | Mostly sitting |
| Physical demands | physical low · computer high |
| Languages | English |
| Education | Master’s degree (required), Doctorate (required) |
| Fields of study | Statistics, Biostatistics, Epidemiology, Computer Science |
Summary and details written by AI from the posting; the employer’s posting is the authority.
Warman O'Brien
| Field | Value |
|---|---|
| Open jobs on Jobsy | 1 |
Senior/Principal Statistical Programmer | Small CRO | Remote/Hybrid
We're partnered with a small CRO who are experiencing a large amount of growth within Biometrics.
The Role: As a Senior Statistical Programmer, you'll lead high-impact projects, tackling complex statistical programming tasks and managing project timelines. You'll work directly with clients and regulatory agencies, ensuring data quality and delivering programming solutions for clinical trials. You’ll also have the chance to mentor junior team members, contribute to regulatory submissions, and develop new programming tools.
Key Responsibilities:
- Lead statistical programming for complex projects, solving intricate challenges while ensuring project delivery meets quality standards.
- Collaborate with clients, providing programming oversight, project estimates, and participating in bid defenses.
- Contribute to regulatory submissions and represent the company in regulatory discussions.
- Create and validate SDTM and ADaM dataset specifications, ensuring adherence to SOPs.
- Program and validate datasets, ensuring accuracy and data integrity.
- Mentor junior programmers and lead project teams, fostering development and collaboration.
- Innovate by developing macros, utilities, and tools to enhance efficiency.
- Implement data integrity checks, ensuring scientific accuracy and quality.
Qualifications:
- Master’s or Ph.D. in Statistics, Biostatistics, Epidemiology, or Computer Science.
- 6+ years of clinical trial statistical programming experience with a Masters Degree or higher in a Statistical related subject.
- Experience working with clinical trial data, SDTM/ADaM datasets, and regulatory submissions.
What to do next?
Apply now to avoid missing out on this opportunity!
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