Senior Statistical Programmer (North America)
Bioforum · Canada, United States · CA,US
Clinical Data Science
Remote
Not yet analysed
Demand78
Career growth72
Healthcare fit58
Remote potential65
5-year outlook
Senior statistical programmers in clinical research are typically well compensated in the US market, with potential to move into principal programmer, biostatistics, or data standards leadership roles. Exact figures vary by employer, location, and therapeutic area.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-09-28
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- Canada, United States
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth applying only if you have strong SAS and CDISC clinical trial programming experience; clinicians without that technical background will likely not be competitive.
Who should apply
Clinicians with prior statistical programming, biostatistics, or clinical data science experience, especially those with SAS, CDISC SDTM/ADaM, and regulatory submission exposure.
CV angle
Frame clinical or research experience around SAS programming, CDISC data standards, TFL development, validation, regulatory submission documentation, and cross-functional collaboration on clinical trials.
Skills to highlight
- SAS programming
- CDISC SDTM/ADaM
- TFL programming
- Define.xml
- Reviewer's Guide
- Clinical trial data analysis
- Validation and QC
- Project management
- Mentoring
Role summary
Senior statistical programmer responsible for SAS programming, CDISC-compliant datasets, TFLs, submission documents, validation, and mentoring within clinical trial projects.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.