Temp Statistical Programmer
Core
Producing or verifying SAS scripts and outputs (tables, listings, figures) for clinical trial analysis files and regulatory submissions.
Role type
Senior Statistical Programmer (Clinical Trials)
Builds
CDISC-compliant SDTM and ADaM datasets, analysis tables, listings, figures, and regulatory submission documents.
Domain
Clinical Research / Biostatistics / Oncology
Required skills
SAS programming, clinical trial data analysis, CDISC standards (SDTM/ADaM), statistical analysis plan review, biometrics quality control, documentation writing
Preferred skills
Oncology experience, innovative technology adoption (via careerplan.io/jobs/gec373e3-temp-statistical-programmer-at-unicon-pharma-inc)
Technologies
SAS, SAP
Responsibilities
Write analysis file specifications and documentation, perform biometrics quality control of clinical-data documents, review statistical analysis plans and documents, program in-house deliverables for dose committees and board meetings, support regulatory submissions and publications, communicate with statisticians and functional groups
Seniority
Senior, hands-on IC