 Advanced knowledge of / experience with SAS and other relevant programming software

 Proven experience in development of advanced MACROs with high programming efficiency;

strong programming and problem-solving skills.

 Proven experience in leading programmer support for multiple clinical trials and submission
activities (or equivalent)

 Must have expertise in SAS/BASE, SAS/MACRO, SAS/STAT, SAS/GRAPH, SAS/ACCESS,

SAS/ODS, SAS/SQL

 Skilled in SAS programming, merging SAS datasets, preparing data, producing and validating
reports, SAS formats, and managing data

 Must have working knowledge in using report generating procedures like PROC CONTENTS,
PROC PRINT, PROC REPORT, PROC TABULATE, PROC FORMAT, PROC FREQ, PROC
UNIVARIATE, PROC SUMMARY, and PROC TRANSPOSE.

 Working knowledge of database design/structures and basic statistics

 Working experience in pooling analysis datasets across multiple clinical studies (or equivalent)

 Good understanding of global clinical trial / project practices, procedures, methodologies

 Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP,

ICH)

 Intermediate knowledge of office tools

 Should have experience with SDTM Implementation and ADaM implementation according to
CDISC Standards

 Must have strong written/verbal communication skills

 Fluent English (oral and written)