Key Duties and Responsibilities :
Displays basic familiarity with many of the SAS procedures and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH Codes SAS programs for applications designed to analyze and report clinical trial data and for electronic submissions of data in CDlSC format with instruction or input from supervisorPerforms quality control checks of SAS code and output produced by other Statistical Programmers to ensure accuracy and consistency within group Demonstrates emerging knowledge of clinical development and medical data Solves straightforward clinical trial reporting problems and has a proven technical proficiency in supporting daily operations and ensuring that project tasks are completed accurately and on schedule under supervision Demonstrates intermediate knowledge of electronic submissions and CDlSC Works with internal staff and external vendors to implement and optimize CDlSC transformation activities Supports daily operations and ensures that project tasks are completed accurately and on schedule.
Knowledge and Skills : Basic SAS Effective Communication (written and verbal) skills, especially within area(s) of expertise.
Education and Experience : Bachelors degree in a Scientific Discipline.
