Join Cytel’s enthusiastic and collaborative Biometrics team by contributing to the overall success of our novel gene therapy development programs. The Sr. Statistical Programmer provides Statistical Programming technical support to team members.

• Effectively designs and codes SAS programs for assigned project(s), consistently meeting objectives of the project

• Codes complex SAS programs for applications designed to analyze and report clinical trial data and for electronic submissions of data in CDlSC format with minimal instruction or input from the supervisor

• Create specifications for derived/analysis datasets Program analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS Generate SDTM domains, ADaM datasets

• Performs quality control checks of advanced SAS code for datasets and output produced by other Statistical Programmers

• Performs review on define.xml and creates reviewers guide for SDTM and ADaM datasets

• Review, and maintain study documents per the standard process

• Perform other duties as assigned

• Demonstrates advanced experience with all SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT, and SAS/GRAPH

• Demonstrates intermediate knowledge of electronic submissions and CDlSC

• Proven technical proficiency in supporting daily operations and ensuring that project tasks are completed accurately and on schedule

• Effective communicator (written and verbal), especially within their area(s) of expertise

Preferred Education And Experience

• MS in biostatistics or a related field, with 5-8 years of experience in the pharmaceutical industry, or BS in biostatistics or a related field, with 7-10 years of experience in the pharmaceutical industry