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Accountabilities / Responsibilities:
Provide input as appropriate into all meetings, discussions and activities covering all SAS programming aspects for assigned clinical trials in the project. Programming of analysis datasets, pooled datasets, listings, summaries, figures and tables for the reporting and analysis of the clinical trials and of the ISS and ISE according to client specifications.
Skills / Qualifications
Expert in CDISC, ADaM and SDTM
Strong SAS programming skills in BASE, MACRO, STAT and GRAPH
Tables, listings, graphs, generating reports and anlysis of reports.
Responsiblity for own projects and documention.
Lead discussions on continuous improvement projects within the statistical programming groups.
For further details and a confidential conversation please contact me directly:
Manager - Statistics, Biostatistics & Programming
Pharmaceutical, Healthcare & CRO Division
Tel: +44 (0) 207 255 6665
Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician
SAS, BASE, MACRO, GRAPH, CDISC, AdaM, SDTM clinical, programmer, analyst, statistical, pharmaceutical