Senior Statistician, CVRM
Core
Senior Statistician leading statistical design, conduct, analysis, and interpretation of clinical trials to ensure scientific rigor and regulatory compliance for drug development.
Role type
Senior IC clinical trial statistician
Builds
Clinical trial protocols, statistical analysis plans, CSR documents, and regulatory submissions
Domain
Pharmaceutical clinical development / Biostatistics
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical trial statistics, SAS, R, CDISC standards, regulatory expectations, statistical methodologies, protocol development, data analysis, result interpretation
Preferred skills
CVRM disease experience, global study team collaboration, mentoring, strategic portfolio-level decision contribution
Technologies
SAS, R
Responsibilities
Lead statistical input into clinical trial design; own development and quality review of statistical study documents; design and execute complex analyses; represent Biostatistics at Study Team level; collaborate with cross-functional teams; interpret and communicate results; lead statistical contributions to CSRs and regulatory documents; provide functional guidance and informal mentoring
Seniority
Senior, hands-on IC with mentoring responsibilities
