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Principal Statistical Programmer /Analyst Consultant -CVRM

UK💼 Full-time🗓 2026-09-17 → 2026-09-26

Core

Lead statistical programming activities for clinical trials, developing SAS programs and datasets, and supporting regulatory submissions.

Role type

Principal Statistical Programmer Consultant

Builds

Production CDISC datasets (SDTM/ADaM) and regulatory submission packages

Domain

Clinical research / Pharmaceutical development

Deliverable

production ML models | product features | dashboards & analysis | client delivery

Required skills

SAS programming, CDISC standards (SDTM/ADaM), regulatory submission support, technical guidance, mentoring, project ownership

Preferred skills

None stated

Technologies

SAS

Responsibilities

Leading statistical programming activities for clinical trials, Developing/reviewing SAS programs and datasets, Providing technical guidance to Statistical Programmers, Reviewing programming specifications and outputs, Supporting SDTM/ADaM and regulatory submissions, Mentoring junior and senior programmers

Seniority

Principal, hands-on IC with mentorship

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