Senior Biometrician @ NOVARTIS -R

Senior Biometrician 
Novartis - Hyderabad, Andhra Pradesh

The Senior Biometrician is responsible and accountable for leading and delivering statistical analytic solutions for multiple Phase I-IV clinical trials at a trial level by executing RAPs, ensuring high quality and timely production of statistical reporting deliverables (tables, listings and graphs), supporting decision making at the CTT/GCT and working together with the statistical scientist and the programmer. They support standardization activities which include aligning activities of the individual studies to a MAP and developing computational solutions which lend themselves to easy standardization across multiple programs. 1.Responsible and accountable for transcribing MAP aligned RAPs into computational solutions for the statistical programmer to implement (specifications of derived variables, specification and development of statistical computing solutions for inferential statistical analyses, tables and listings templates, and modern statistical graphics for the FIR and CSR) of Phase I-IV clinical trials. 2.Responsible and accountable for multiple studies RAP execution including the RAP meetings with the necessary CTT members, reporting activities, exploratory analyses/ graphics and additional analyses to support publications for individual clinical trials. 3.Ensure that documents, specifications, programs/macros are consistent and comply with CSU/project/company standards/processes and provide operational input into VAPs, specifications of analysis datasets, listings, tables and figures, CSR for Phase I-IV clinical trials ensuring that consistent practices across multiple studies is kept 4.Ensure high quality for all assigned deliverables and processes and ensure audit-readiness. 5.Ensure to deliver agreed timelines for statistical deliverables. 6.Establish and maintain efficient interfaces with internal and external customers with support of IIS management. 7.Support statistical research by providing advice and solutions on computational aspects of the problem. 8.Provide statistical analysis solutions when exploratory analyses are required. 9.Attend CTT/GCT meetings to help facilitate decision making during design, conduct and reporting of clinical results 10.Contribute to change initiatives 11.Contribute to project level activities  Minimum requirements  MS (in Statistics or equivalent) with 2+ years relevant work experience or PhD (in Statistics or equivalent) with no work experience Fluent English (oral and written). 1. Working knowledge of/experience with SAS/ R/ Splus or any other business or research analytic software with an expertise in at least one software. 2. Statistical and numerical knowledge and expertise in analytic aspects. 3. Good knowledge of data architecture 4. Excellent nterpersonal and communication skills CLICK HERE TO VIEW/APPLY JOB