Senior Statistical Programmer - 6-month contract, fully remote (US), W2
$70/hr A commercial-stage oncology biotech needs an experienced SAS programmer to support the clinical study report for a randomized Phase III study. You will independently develop, validate and document SAS programs for ADaM datasets and tables, listings and figures in line with the SAP, CDISC standards and ICH guidance.
What you'll do
Program and validate ADaM datasets and TLFs for the CSR, including efficacy figures
Develop and validate SDTM/ADaM specifications and datasets; review SAPs, aCRFs and specs
Support regulatory deliverables and ad hoc analyses
Work directly with biostatistics and cross-functional partners
What you bring
6+ years of SAS programming in pharma, biotech or a CRO
Strong CDISC: SDTM, ADaM, define.xml
CSR or regulatory submission experience (NDA/sNDA, IB, DSUR)
SAS/BASE, SAS/STAT, SAS/SQL, SAS/GRAPH, SAS Macro
Oncology experience preferred: time-to-event endpoints, RECIST, Kaplan-Meier and forest plots
BS/MS in Statistics, Mathematics, Computer Science, Engineering or related; MS preferred
W2 only. Start as soon as possible.