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Position: Senior Statistician - Late Oncology
Institution: AstraZeneca
Location: Barcelona, Catalonia, Spain
Duties: Provide statistical leadership in support of the Global Product Statistician (GPS), be a newly appointed GPS, or lead strategic capability or business area improvements with minimal supervision; Serve as primary author for statistical sections of protocol concept sheets (PCS), protocols, clinical development plans (CDP), and integrated product development plans (iPDP); Perform statistical analyses and create statistical text for clinical publications and other communications; Provide direction and statistical oversight to outsourcing partners/providers regarding requirements and standards for study-level work, holding partners/providers accountable for the quality of their deliverables; Define and lead analysis of relevant internal and external information to inform design decisions; Provide statistical support and leadership to clinical trial teams (CTT), clinical sub-teams (CST) and product development teams (PDT) on the development of Target Product Profile and Target Product Claims (TPP/TPC), Benefit, Risk, Value and Uncertainty (BRV(U)), clinical development plans (CDP), and regulatory strategy
Requirements: MSc/PhD in Statistics or Mathematics (containing a substantial statistical component) with experience in pharma/healthcare or other relevant area; In depth knowledge of the technical and regulatory requirements related to the role; Expert leadership capabilities to be able to lead and direct project work; Extensive experience of Development, programme design and data analysis and interpretation
   
Text: Senior Statistician - Late Oncology Provide statistical leadership in support of the Global Product Statistician (GPS), be a newly appointed GPS, or lead strategic capability or business area improvements with minimal supervision; Serve as primary author for statistical sections of protocol concept sheets (PCS), protocols, clinical development plans (CDP), and integrated product development plans (iPDP); Perform statistical analyses and create statistical text for clinical publications and other communications; Provide direction and statistical oversight to outsourcing partners/providers regarding requirements and standards for study-level work, holding partners/providers accountable for the quality of their deliverables; Define and lead analysis of relevant internal and external information to inform design decisions; Provide statistical support and leadership to clinical trial teams (CTT), clinical sub-teams (CST) and product development teams (PDT) on the development of Target Product Profile and Target Product Claims (TPP/TPC), Benefit, Risk, Value and Uncertainty (BRV(U)), clinical development plans (CDP), and regulatory strategy MSc/PhD in Statistics or Mathematics (containing a substantial statistical component) with experience in pharma/healthcare or other relevant area; In depth knowledge of the technical and regulatory requirements related to the role; Expert leadership capabilities to be able to lead and direct project work; Extensive experience of Development, programme design and data analysis and interpretation
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