▷ (Urgent) Senior Statistical Programmer

24 hours ago

India Capgemini Engineering Full time

NOTE - - Looking for only 7+yeras of experience. - This Job requires you to work from PAN India Capgemini office. JOB DESCRIPTION The Statistical Programmer II (SP II) - Programs all tables, listings and graphs necessary for an assigned clinical study report (CSR); - Programs customized data displays, (including data listings, summary tables and routine graphics) in accordance with the approved statistical analysis plan (SAP) and shell displays for clinical research studies; - Writes code using Base SAS programs, SAS procedures, or standardized macros; - Analyzes protocol, SAP, existing shells/templates as needed to understand structure and content of data; - Performs data checks as needed, to ensure integrity and correctness of data displays; - Prepares documentation for programs; - Prepares documentation describing all datasets and variables within, including derived variables, and the project as a whole; - Creates SAS datasets of clinical data from clinical databases; - Creates status and efficacy datasets; - Creates project-specific macros and formats; - Loads client data from other platforms and other software packages; - Prepares data to be sent to clients and as needed for other external transfers and data imports. - Assists manager and/or director to keep track project timelines and deliverables; - Leads junior programmers in daily activities and performs on-the-job training to them; - Communicates with clients for risks, issues, and potential delays QUALIFICATION FOR ESSENTIAL FUNCTIONS - Ability to communicate effectively in English, in both writing and verbal. - Ability to learn quickly and pay attention to details. - Ability to manage multiple tasks/projects, effectively prioritize and execute tasks, and make quality and on time deliveries. - Ability to work collaboratively, effectively, and productively in diverse organizational structures, and in interaction with dynamic clients. - Ability to work independently, takes ownership and strives for quality and efficiency. - Ability to work positively in a continually changing environment. - Solid/Advanced SAS skills and understanding of the concept of standardization in data, programming, and statistical reporting of trial results and its implication to drug development. EDUCATION AND EXPERIENCE REQUIRED - Bachelor's degree, but Master's degree or above, is preferred, in Biostatistics, Computer Science, Mathematics, or a combination of education and relevant industry experiences. - Strong SAS programming language and good knowledge/experiences of clinical trial and drug development. - At least 8 years of clinical programming or SAS programming experiences for the SP II position.

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