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Senior Biostatistician (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Consultants
Projektbeschreibung
REFERENZNUMMER:
321316/11
IHRE AUFGABEN:
-You will develop and maintain timely, scientifically sound, innovative and business-oriented plan for the statistical analysis and data management of clinical studies
-Develop, execute or supervise appropriate statistical analyses of clinical trial data
-Manage consultants and outside collaborators that provide statistical and data management (Umbrella only) expertise for individual tasks or entire studies
-Act as liaison between external contractor and team
-Keep abreast of statistical methodological developments through literature and attendance at meetings
-Keep abreast of regulatory authority guidelines relating to biostatistics and with medical issues in own project areas
IHRE QUALIFIKATIONEN:
-PhD or at least MSc (diploma) in statistics or mathematics
-Good knowledge of the drug development process, GCP and regulatory guidelines, statistical methods for Health Outcome studies, SAS and other statistical software packages
-Good knowledge of the CRO business with a special focus on statistics and data management services provided
-Profound experience working as a statistician in the pharmaceutical industry or in CROs
-Successful statistical project management and leadership skills acquired within the pharmaceutical industry or in CROs
WEITERE QUALIFIKATIONEN:
Biostatistician
321316/11
IHRE AUFGABEN:
-You will develop and maintain timely, scientifically sound, innovative and business-oriented plan for the statistical analysis and data management of clinical studies
-Develop, execute or supervise appropriate statistical analyses of clinical trial data
-Manage consultants and outside collaborators that provide statistical and data management (Umbrella only) expertise for individual tasks or entire studies
-Act as liaison between external contractor and team
-Keep abreast of statistical methodological developments through literature and attendance at meetings
-Keep abreast of regulatory authority guidelines relating to biostatistics and with medical issues in own project areas
IHRE QUALIFIKATIONEN:
-PhD or at least MSc (diploma) in statistics or mathematics
-Good knowledge of the drug development process, GCP and regulatory guidelines, statistical methods for Health Outcome studies, SAS and other statistical software packages
-Good knowledge of the CRO business with a special focus on statistics and data management services provided
-Profound experience working as a statistician in the pharmaceutical industry or in CROs
-Successful statistical project management and leadership skills acquired within the pharmaceutical industry or in CROs
WEITERE QUALIFIKATIONEN:
Biostatistician
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Organisation/Management