Expert knowledge of clinical trial data analysis processes and SAS programming
Excellent knowlegde of implementing CDISC Standards - SDTM, ADaM, Creation of SDRG, ADRG, Define.xml
Prior strong experience in one or two therapeutic areas
Prior experience of working on analysis of both safety and Efficacy data
Prior experience of leading the studies and managing a team of 5-8 programmers
Prior of experience of creating or maintaining system-level macros
Prior experience of working with study deliverables like DMC, QRS, ASCO, BDR, CSR, Interim CSR
Project management skills, including time management, planning, work allocation and project delivery
Ability to coordinate with all functional areas that make up a clinical project team and to interface with different cultures, both internally and externally.
