Use efficient programming techniques to produce and QC of derived datasets and TLF.
Create/modify standard macros and applications to improve the efficiency.
Develop wider knowledge of SAS and other relevant programming languages and processes.
Understanding regulatory requirements concerning industry technical standards, maintain all supporting documentation in accordance with WSOPs/guidelines.
A graduate or master degree in a relevant educational filed life science, computer, pharmacy, others.
Proficiency in SAS and knowledge of programming and reporting process.
Excellent experience with TLF, SAS coding, Macros, SQL, PROC reports, SDTM, ADAM (preferred)
Knowledge of WSOPs/ICH-GCP and System Life Cycle methodologies.
Excellent communication (written & oral) skills and strong leadership ability.
Strong organizational skills, flexible to change and team work.
Data conversions and transfers.
Working knowledge on Windows/Unix Environment
Working knowledge on SAS migration projects of moving files from one location of the server to another Example SAS 9.2 to 9.3 or 9.4
Proficiency in SAS
Knowledge of programming and reporting processes
Commitment to consistent high quality of work in a regulated industry
Demonstrate strong organizational skills and ability to manage activities related to their assigned task
Experience with Windows PC and Microsoft Office applications
Understanding of Unix commands, file systems, and shell scripts
Coordinate study programming activities with peer staff
Understands quality and regulatory requirements with ability to identify risk potential from programming activities