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Position: Principal Biostatistician, Biometrics
Institution: Vertex Pharmaceuticals
Location: Boston, Massachusetts, United States
Duties: Conducts advanced scientific and operational statistical work for multiple clinical trials, observational studies, or real world data (RWD) investigations, including the design, development and execution of the technical/statistical infrastructure; Possesses an advanced understanding of modern drug discovery and development processes; Represents Biostatistics as a member of clinical trial teams, providing input and technical guidance to elicit meaningful and/or productive outcomes; With minimal guidance, authors study Statistical Analysis Plans (SAPs), including table, figure, and listing (TFL) shells. Develops Cross-functional Data Review (xFDR) plan, Key Reports Memo (KRM), and Data Dissemination Plan (DDP) to facilitate the review, summary, and dissemination of key study data/results; Collaborates with statistical programming and other functions to ensure timely delivery of TFLs with good quality
Requirements: Ph. D. or master's degree in Statistics or Biostatistics; Typically requires 3 years of experience with a Ph.D. or 6 years of experience with a master's degree, or the equivalent combination of education and experience
   
Text: Principal Biostatistician, Biometrics Conducts advanced scientific and operational statistical work for multiple clinical trials, observational studies, or real world data (RWD) investigations, including the design, development and execution of the technical/statistical infrastructure; Possesses an advanced understanding of modern drug discovery and development processes; Represents Biostatistics as a member of clinical trial teams, providing input and technical guidance to elicit meaningful and/or productive outcomes; With minimal guidance, authors study Statistical Analysis Plans (SAPs), including table, figure, and listing (TFL) shells. Develops Cross-functional Data Review (xFDR) plan, Key Reports Memo (KRM), and Data Dissemination Plan (DDP) to facilitate the review, summary, and dissemination of key study data/results; Collaborates with statistical programming and other functions to ensure timely delivery of TFLs with good quality Ph. D. or master's degree in Statistics or Biostatistics; Typically requires 3 years of experience with a Ph.D. or 6 years of experience with a master's degree, or the equivalent combination of education and experience
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