Principal Statistical Programmer /Analyst Consultant -CVRM
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