CTC Clinical Trial Consulting AG C

Senior Biostatistician (BB-2454A)

Gefunden in: Xpatjobs CH

Main Responsibilities: Provide input in the evidence development strategy of projects (including design, sample size, modelling/simulations) by evaluating scientific background knowledge.Coordinate regular and complex statistical tasks with high level of autonomy with high level of autonomy and ensure the activities performed throughout a trial are compliant with current guidelines and processes.Provide statistical input for protocol writing review of clinical study documents.Responsible for statistical analysis strategies ensuring their feasibility, efficiency, validity and reproducibility.Write and review statistical analysis plans and ensure agreement with protocol whilst also ensuring their feasibility, efficiency, validity and guidelines-adherence (GCP)Analyse clinical data and present statistical results.Responsible for statistical aspects if scientific communication on clinical projects. Qualifications and Experience: Masters or PhD in a field relevant to Biostatistics.Minimum 10 years of experience in academia or industry as a Biostatistician.Comprehensive knowledge of biostatistics in all phases of clinical development, in particular in the planning, execution, analysis and reporting of clinical studies.Proficiency with various statistical methodologies applied in clinical trials and knowledge of regulatory guidance.Knowledge in Bayesian statistics and / or adaptive design methodology.Strong analytical and organizational skills.Ability to work on multiple assignments at the same time.Good communication skills towards both scientific and business partners.

calendar_todayvor 4 Tagen


location_on Lucerne , Lucerne, Schweiz

work CTC Clinical Trial Consulting AG

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