Statistical Programmer Consultant
Kyverna · United States · US
Clinical Data Science
Remote
Not yet analysed
Demand78
Career growth70
Healthcare fit35
Remote potential95
Salary band
USD 80 – 100
5-year outlook
Senior statistical programming skills, especially SAS and CDISC submission experience, remain valued in biopharma and CROs. The posted $80–100/hr rate reflects a senior contract level, but the 6-month term means income stability depends on renewal or follow-on contracts.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
contract
Date found
2026-10-18
Intelligence details
Flexible work details
- Engagement type
- Temporary
- Hours
- Variable hours
- Eligible countries
- United States
- Rate period
- Hourly
Why this was classified this way
- Temporary
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 considering only if you already have 8+ years of statistical programming in pharma/CRO and strong SAS/CDISC submission experience. Most clinicians without that technical background should not prioritize this role.
Who should apply
Experienced statistical programmers or biostatisticians with clinical trial and regulatory submission experience; clinicians who have transitioned into biostatistics or clinical data science and can evidence SAS, SDTM/ADaM, and TLF work.
CV angle
Lead with SAS programming, CDISC SDTM/ADaM, TLF generation, define.xml/Pinnacle 21, and regulatory submission deliverables. Frame clinical research or data-management experience as transferable only where you actually performed programming, validation, or cross-functional trial support.
Skills to highlight
- SAS programming
- CDISC SDTM/ADaM
- Tables, Listings, and Figures (TLFs)
- define.xml
- Pinnacle 21
- Regulatory submissions/eCTD
- Clinical trial data validation
- Cross-functional collaboration
Role summary
A senior contract statistical programmer who leads SAS programming for clinical trials, builds and validates SDTM/ADaM datasets and TLFs, and prepares CDISC/regulatory submission packages for a cell therapy company.
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