Senior Programmer I/II (Oncology)
Core
Senior SAS programmer responsible for statistical programming, database setup, and regulatory submission support for oncology clinical studies.
Role type
Senior IC clinical data programmer (SAS)
Builds
SDTM and ADaM databases, statistical reporting outputs (TFLs), and regulatory submission packages
Domain
Pharmaceutical / Oncology / Clinical Data Management
Required skills
SAS programming, CDSIC standards, database setup, statistical concepts, regulatory requirements, project management
Preferred skills
R, S-PLUS, Python, XML
Responsibilities
Review study documents (CRF, SAP, validation plans), program and validate SDTM/ADaM databases, communicate technical requirements to vendors, mentor junior staff, contribute to regulatory submission packages
Seniority
Senior, hands-on IC
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