Technical Lead SAS Programming

Experience: 5-13 years Relevant in Clinical SAS Programming Roles and Responsibilities: Programming 1) Primarily responsible for quality and timely delivery of ADaM artifacts (Specifications, datasets, ADRG) and TFLs 2) Read and understand Clinical study protocol, Statistical Analysis Plan, Case Report Form (CRF), specifications and other study related documents. 3) Develop SAS programs to produce Analysis datasets, statistical tables, graphical representations, and data listings for individual study reports in accordance with the Statistical Analysis Plan (SAP) 4) Develop validation programs to validate outputs produced by other team members and perform validation on program code of other team members. 5) Provide support to Data Management in developing Edit check programs, listings or ad hoc reports as required 6) Develop, Debug Utility macros for reusability and efficiency Customer & Delivery Management 1) Support & Supervise Programming team towards resolving study/program related issues and thereby efficiently meet all project timelines & deliver quality outputs. 2) Respond to queries raised by sponsor/regulators 3) Communicate with project team/stakeholders/ other departments and/or groups effectively