Role
Develop and maintain databases under SAS and Macro
Develop consistency programs under SAS and Standardizing SAS programs.
Develop reports, listings, tables and figures.
Assist data-managers and Statisticians in the maintenance and update of programs Working on SAS Procedures like PROC FREQ, PROC SUMMARY, PROC TRANSPOSE, PROC IMPORT,
PROC EXPORT, PROC SORT, PROC FORMAT, PROC SQL, PROC REPORT, PROC TABULATE.
Working on functions (SCAN, SUBSTR UPCASE, TRANSLATE, PUT, INPUT etc.),
statements (Input, Infile, Keep, Drop, label etc. and automatic variables (first, last variable, _null etc.).
Working on Macros and automation, variable creation, utility macro writing etc.
Keeping up to date with Clinical domain knowledge understanding Protocol, SAP, Clinical domain knowledge, well versed with standard clinical trials domains like events (Adverse Event, Concomitant medications),
finding domains (vitals, labs, etc.) and well versed with annotated CRF's.
Support the Quality Management System (QMS) by participating in the life cycle of procedure and other applicable documents, declaring non-compliances encountered in the daily operations and following the associated corrective and preventive plans.
Experience in a CRO, Institute or Research centre.
Office based in a desirable location in Paris.
