Statistical Programmer
Core
Statistical Programmer analyzing and reporting clinical trial data to support the R&D of new pharmaceutical products.
Role type
Mid-level IC statistical programmer (clinical data)
Builds
ADaM data sets, Tables, Listings, Figures, and regulatory documentation for clinical studies
Domain
Pharmaceutical clinical trials / CDISC standards
Required skills
SAS programming, CDISC standards (ADaM), data consolidation, exploratory data analysis, data visualization, validation of data sets and outputs
Preferred skills
NONMEM concepts and techniques
Technologies
SAS, NONMEM
Responsibilities
Create documentation for regulatory filings including reviewers guides and data definition documents; Consolidate heterogeneous data sources to prepare analysis-ready data sets; Develop SAS programs for the creation of ADaM data sets, Tables, Listings and Figures; Validate ADaM data sets, Tables, Listings and Figures; Create specifications for the structure of ADaM data sets for individual studies
Seniority
Mid-level, hands-on IC