NOVARTIS hiring Statistical Programmer in Hyderabad, Telangana


Statistical Programmer

Job Description
Your responsibilities:
Your responsibilities include, but are not limited to:


1. Provide input as required at all meetings, discussions, and activities covering aspects of Statistical Reporting on trial level activities.
2. As required, make certain that documents and specifications are consistent and comply with company standards for specifications of analysis datasets, listings, summaries, figures and tables for phase I – IV clinical trials.
3. The program, according to specifications, analysis datasets, listings, tables, and figures for phase I-IV clinical trials and/or apply standard statistical methods (as Reporting Statistician in Phase I) to standardized PK study designs.
4. Track clinical trial milestones for ONC Biometrics deliverables.
5. Maintain records for all assigned deliverables including archiving of trial analysis and associated documentation. Comply with pre-defined project/study standards and specifications.
Minimum requirements
• BA/BS/MS or international equivalent experience in statistics, computer science, mathematics, life sciences or related field Fluent English (oral and written).
• Basic SAS experience within a Statistical Programming environment to develop and validate deliverables
• Basic experience in contributing to statistical analysis plans and/or constructing technical programming specifications
• Basic understanding of regulatory requirements relevant to Statistical Programming (e.g. GCP)
• Basic communications and negotiation skills, ability to work well with others globally
• Ideally 2+ years of work experience in a programming role



Comments

Popular posts from this blog

Job Openings for Clinical Data Analyst II in Cytel Pune, Maharashtra, India