HTA Statistician (m/f) 395364/11

März 2019

Februar 2020


nicht angegeben




Ihre Aufgaben:
Provide expert statistical and programming support as well as methodological advice to facilitate the generation of evidence used for market access and reimbursement submissions
Perform statistical analyses on clinical trial and real-world data, including analysis of efficacy, safety, quality of life and utility endpoints
Provide input into clinical development and access evidence plans
Provide input into design of experiments including clinical trials and patient registries with a particular focus on the analysis of payer-relevant endpoints
Provide expert statistical advice on statistical methodologies as well as the interpretation of statistical findings
Work collaboratively with colleagues across the Roche global organization as well as country-level affiliates to support and ensure appropriate generation, synthesis and interpretation of payer-relevant evidence

Ihre Qualifikationen:
Previous working experience as Statistician in a pharmaceutical environment
Very good knowledge of R or SAS programming, knowledge of other software such as Stata, WinBUGS and/or JAGS as well as prior experience working with Unix environment and GitHub would be a plus
Previous experience in modelling survival data
Good knowledge of the following aspects: drug development, clinical development plans, design of experiments for clinical trials and registries, access evidence plan
Organizational and project management skills (including vendor management) would be a plus

Projektstart: 03/19
Projektdauer: 12 MM++

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