Senior Statistical Programmer II
Core
Lead statistical programming and analysis activities for clinical study reports and regulatory submissions in oncology drug development.
Role type
Senior Statistical Programmer (Oncology)
Builds
Clinical Study Reports (CSRs) and regulatory submissions for oncology products
Domain
Pharmaceutical / Clinical Trials / Oncology
Deliverable
production ML models | product features | dashboards & analysis | client delivery
Required skills
Advanced SAS programming, CDISC standards, clinical trial study leadership, regulatory compliance knowledge, stakeholder management
Preferred skills
Oncology therapeutic area experience, submission experience
Technologies
SAS
Responsibilities
Develop clinical study reports, lead statistical programming activities for regulatory submissions, manage concurrent studies, influence team members on technical and regulatory requirements
Seniority
Senior, hands-on IC with leadership responsibilities
