Informacje podstawowe

Opis zadania i wymagań

Tasks:
• Conduct statistical analyses for Global Medical Affairs and HEOR in Quizartinib by means of:
• Preparation and review of analysis documentation (SAP, TFLS shells, List of Outputs, Derivation details)
• Development and maintenance of programs to create or validated analysis datasets, tables, figures and listing as per analysis requirements
• Ensure that the analysis will meet expectations in term of timeliness and quality
• The analyses are primarily used for publications, abstracts, presentations and conferences as well as regulatory/pricing submissions

Requirements:
• Bachelor's degree in statistics, biostatistics, mathematics, computer science or life sciences; master's degree in bio/statistics preferred would be benifical
• Experience supporting drug development and/or post marketing in clinical research, Pharmaceutical. CRO or Medical Device setting
• Experience in oncology OR cardiovascular therapeutic Area and/or in late phase projects is an advantage
• Excellent English language skills
• Good understanding of GCP and GDPR principles
• Advanced working knowledge all SAS language, procedures and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH.
• Knowledge of SAS Enterprise Guide and/or SAS Studio is recommended but not required
• Previous experience supporting SAS macro and/or system utility development is preferred
• R knowledge is highly recommended .
• Ability and interest to work remotely with worldwide team members across cultures and time zones

Advantages:
• Remote possibility
• Long duration
• International team

Duration: 8 MM

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