Description
JOB RESPONSIBILITIES:* Gathers requirements for assignments, and executes those requirements
* Integrates data from various sources for use in validating trials
* Documents and validates results generated
* Oversee CRO programming activities
* Generates assorted tables and analyses as required for internal and external use
* Writes and checks codes written by SAS Statistical Programmer(s) to be used for statistical programs and performs quality control checks to ensure codes work according to program design
* Reviews table figures and set-up to look for inconsistencies and correct if any are found
JOB REQUIREMENTS:
Education
* Master's degree is required.
Experience
* Minimum of five (5) year's relevant SAS programming in a biotechnology or pharmaceutical company
* SAS Certification desirable, Proficiency in Excel and Word
*Experience working on NDA submissions
*Oncology background
To find out more about Real please visit www.realstaffing.com