Job Description :
MS in Biostatistics/Statistics preferred, with at least 5 years of experience in the pharmaceutical, CRO or biotech industry.
Strong SAS programming skills, with experience in SAS-Base, MACRO, STAT, and GRAPH.
Strong CDISC data standards, e.g. SDTM and ADaM.
Ensures timely creation of TLF package and/or submission data/analysis documentation package according to regulatory guidelines.
Proven experience with UNIX and Windows operating systems
             

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