Permanent Biostatistician

Your responsibilities are as follow:

•You will be in charge of the treatment of all statistical methodology questions related to newly certified products
•You will plan the international study programs and studies of the phase IIIb/IV
•You will review the statistics methodology of the statistical analysis plan and reports
•You will be in charge of the writing of risk management plans and you will report in the context of the Pharmacovigilance
•You will work on ad-hoc Safety analyses and Meta analyses
•You will also plan and execute exploratory analyses of existing study databases for the global publication strategy as well as for all aspects of the Life Cycle management of a project
•You will cooperate with the strategy and review of product dossiers to the reimbursement of costs (patient-relevant use & Health Technology Assessments)
•You will provide statistical consultancy for all the aspect of the project and cooperate in international project teams as well as with co-operation with other companies or with external key opinion leaders
•You will collaborate on the writing and review of publications, literature, posters…

Requirements:

•MSc or PhD in Statistics, Biostatistics or Mathematics
•Strong expertise in statistical methodology
•3 to 8+ years professional experience as a Biostatistician within the pharmaceutical, CRO or academic industry
•Excellent knowledge of statistical tools such as SAS
•Proven experience in writing and reviewing publications, lectures, posters…
•Experience with working on submission
•Fluent in English language

If you are the right candidate for this role, Please contact Louise Beka by phone or send me your CV with a cover note by email