Senior Statistical programmer

• Work with Leads statistical programmer on activities for assigned clinical development studies and programs.
• Ensures timely statistical analyses of clinical data per protocols and Statistical Analysis Plans; either directly or through CRO oversight develops statistical programs and produces programmed outputs used to create integrated scientific reports for clinical trial results
• Interacts with CROs involved in data management/analysis activities to ensure that their statistical analyses and resulting outputs are accurate and consistent with the contractually agreed upon deliverables; works with vendor staff to characterize and resolve issues related to data analysis.
• Creates/Reviews derived dataset specifications and the related analysis datasets.
• Performs other tasks and assignments as needed and specified by management.

Requirements:

• Minimum of 6 years of experience in statistics or statistical programming in a pharmaceutical, biotechnology, CRO or related environment.
• Demonstrated and applied SAS programming skills (e.g., Base SAS, SAS/Stat, SAS/Graph, SAS macros, ODS) and a good understanding of database systems.
• Clinical Data Interchange Standards Consortium (CDISC) experience
• Knowledge of clinical data analysis and reporting process as it relates to drug development.
• Excellent verbal and written communication and skills.
• Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.