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Position: Biostatistics Manager
Institution: Amgen Inc.
Location: United Kingdom
Duties: Achieve results through detailed goal setting, accountability measures, effective partnership, performance management, collaboration with other groups and a dedication to serving customers, both inside and outside of CfDA (Center for Design & Analysis); Influence and supply to strategy development, defend statistical approaches and represent GBS (Global Biostatical Science) through participating in and collaborating with multidisciplinary study teams; Provide statistical contributions, statistical review, and quality control of Key Design Elements (KDE) protocols, randomisation specifications, Statistical Analysis Plans (SAPs), Table, Listing and Figure (TLF) shells, Submission Data File (SDF) specifications, other key study related documentation, protocol deviations, Flash Memos, Clinical Study Reports (CSRs), clinical publications, and other communications
Requirements: Degree educated in Statistics/Biostatistics or related subject with high statistical content; Post-graduate statistical experience in the pharmaceutical industry or medical research; Knowledge of SAS, R or other statistical software; Excellent communication skills and ability to work optimally within teams while also possessing the capacity to autonomously manage tasks and projects
   
Text: Biostatistics Manager Achieve results through detailed goal setting, accountability measures, effective partnership, performance management, collaboration with other groups and a dedication to serving customers, both inside and outside of CfDA (Center for Design & Analysis); Influence and supply to strategy development, defend statistical approaches and represent GBS (Global Biostatical Science) through participating in and collaborating with multidisciplinary study teams; Provide statistical contributions, statistical review, and quality control of Key Design Elements (KDE) protocols, randomisation specifications, Statistical Analysis Plans (SAPs), Table, Listing and Figure (TLF) shells, Submission Data File (SDF) specifications, other key study related documentation, protocol deviations, Flash Memos, Clinical Study Reports (CSRs), clinical publications, and other communications Degree educated in Statistics/Biostatistics or related subject with high statistical content; Post-graduate statistical experience in the pharmaceutical industry or medical research; Knowledge of SAS, R or other statistical software; Excellent communication skills and ability to work optimally within teams while also possessing the capacity to autonomously manage tasks and projects
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