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Projektbeschreibung
-Responsible for all statistical tasks for assigned clinical trials in the Oncology therapeutic area, including: protocol writing, analysis planning and reporting, exploratory analyses, publication support, and statistical consultation
-Coordinate study tasks with other statisticians and statistical programmers
-Ensure timeliness and adequate quality of all statistical deliverables
-Follow processes and project standards as well as Health Authority requirements
-MSc in statistics
-Profound experience in pharmaceutical development and clinical research
-Strong statistical skills and knowledge of clinical trials methodology: experience with protocol development, analysis planning and reporting of clinical trials
-Knowledge of SAS
-Fluent in English, good oral and written communication skills
-Experience in Oncology clinical trials
Weitere Qualifikationen: Biostatistician
-Coordinate study tasks with other statisticians and statistical programmers
-Ensure timeliness and adequate quality of all statistical deliverables
-Follow processes and project standards as well as Health Authority requirements
-MSc in statistics
-Profound experience in pharmaceutical development and clinical research
-Strong statistical skills and knowledge of clinical trials methodology: experience with protocol development, analysis planning and reporting of clinical trials
-Knowledge of SAS
-Fluent in English, good oral and written communication skills
-Experience in Oncology clinical trials
Weitere Qualifikationen: Biostatistician
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges