Senior Programmer I/II (Oncology)
Core
Senior SAS programmer responsible for statistical programming, database construction, and regulatory submission support within the oncology therapeutic area.
Role type
Senior IC clinical data scientist (SAS)
Builds
SDTM and ADaM databases, statistical reporting outputs (TFLs), and regulatory submission packages
Domain
Pharmaceutical / Oncology / Clinical Data Management
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure
Required skills
Advanced SAS programming, CDSIC standard compliance, database setup, statistical concepts, regulatory requirements knowledge, project management, quality review
Preferred skills
R, S-PLUS, Python, XML
Technologies
SAS, CDSIC, SDTM, ADaM, TFLs
Responsibilities
Plan, lead, and perform quality review of statistical programming study deliverables; Program and validate deliverables for ad hoc analyses and regulatory queries; Communicate technical requirements to biometrics vendors; Mentor and coach junior staff; Contribute to the preparation of regulatory submission packages
Seniority
Senior, hands-on IC with mentorship responsibilities
