Senior Biostatistician And Sas Programmer - Es Madrid Indiferente

  • Confidencial
  • Madrid
  • 09-10-2016
  • Otros
Global provider of product development and support services to the pharmaceutical, biotechology and medical industriesMaintain awareness of statistical issues relating to the design and analysis of the clinical trial, including general issues, regulatory views and Sponsor specific activities.To be responsible for all aspects of statistical input for the design, analysis and reporting of allocated projects according to contracted services in compliance with current legislation, ICH Guidelines and appropriate company/Sponsor procedures and quality standards.Participates within the Biostatistics team for completion of all biostatistics tasks to ensure that they are completed to required quality within the timelines for allocated projects according to contracted services.Active participation in communications with other project teams, principally with the project manager. Main point of contact for sponsor.Preparation of the Statistical Analysis Plan, including template tables, listings and figures, in accordance with Linical SOPs, Sponsor specifications and Industry Guidelines.Quality control of statistical output produced by other members of the department, including tables, listings, figures, derived datasets and statistical analyses.Defines criteria for different populations for the analysis Safety, ITT, PP and perform the programming for the implementation of the criteria.This role offers a broad range of responsibility, variety, challenges and scope for continuing your professional development within a supportive and forward-thinking team environment.

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