descriptionPRINCIPAL STATISTICAL SAS PROGRAMMER ANALYSTKey

Responsibilities

The Principal Statistical Programmer Analyst will have several years experience working as a Statistical Programmer.

• The incumbent will develop SAS codes to create accurate, complete and efficient statistical analysis datasets; and to generate statistical analysis output tables, listings and graphs.
• Creating SDTM and ADaM datasets using CDISC standards.Quality control programming validation procedures will be performed and documented by the incumbent.
• The incumbent will also program for database integrity checks and work closely with Clinical Data Managers and Quality Assurance personnel to assure database quality.
• Additionally, the incumbent will resolve complex programming problems and provide oversight to other Statistical Programmers; lead efforts in the development, maintenance and adherence of Corporate policies, SOPs, and therapeutic area specific guidelines; may act as a Lead/Liaison Programmer, interacting with clinical trial sponsors and oversee projects in given therapeutic areas.
• Qualifications And ExperienceA masters degree in Statistics, with at least 10 years experience in support of clinical trial data analysis and reporting, and demonstrated leadership ability to effectively manage statistical programming activities and integrate them with the entire clinical trial operations.
• Excellent knowledge of drug development process and regulatory requirements including ICH/GCP guidelines and CDISC standards.
• Extensive experience using SAS programming along with experience with SAS/Base, SAS/Macros, SAS/ Graph and SAS/Stat to process, report, and analyze clinical trial data in UNIX operating system