Statistical Programmer

Role: - Clinical SAS Programming

Title - Senior Technical Lead/Technical Lead

Relevant Experience -7 -10 years

Role and Responsibilities

Primarily responsible for quality and timely delivery of Safety & Efficacy SDTM, Adam artifacts (Specifications, datasets, ADRG), and TFLs.

Read and understand Clinical Study Protocol, Statistical Analysis Plan, Case Report Form (CRF), specifications and other study-related documents.

Develop SAS programs to produce Analysis datasets, statistical tables, graphical representations, and data listings for individual study reports per the Statistical Analysis Plan (SAP)

Develop validation programs to validate outputs produced by other team members and perform validation the program code of other team members.

Support Data Management in developing Edit check programs, listings or ad hoc reports as required.

Develop and debug Utility macros for reusability and efficiency.

Customer & Delivery Management Support & Supervise the Programming team towards resolving study/program related issues and thereby efficiently meet all project timelines & deliver quality outputs.

Respond to queries raised by sponsors/regulators.

Communicate with project team/stakeholders/ other departments, and/or groups effectively.