Integrated Analysis Statistician (m/f)

.pre {white-space: pre-wrap;} Your tasks and responsibilities

 

  • Provide statistical input to clinical project teams for designing, planning and conducting post-hoc analyses of existing clinical trial databases and

meta analyses for the assessment of efficacy, safety and benefit risk

  • Develop statistical analysis plans for integrated summaries (e.g. for submissions to regulatory agencies)
  • Support generation of publications, presentations and posters based on integrated analyses
  • Lead (virtual) cross-functional teams of statisticians, statistical analysts as well as data integration specialists
  • Support standardization of data base structures and implement standard processes for integrated analyses
  • Be responsible for the production and accuracy of the statistical analysis as well as interpretation of the results
  • Guide and collaborate with contract research organizations to ensure outsourced statistical work is in alignment with established data, analysis,

quality standards and timelines

 

.pre {white-space: pre-wrap;} Who you are

 

  • Master’s degree/PhD degree in (bio-)statistics or mathematics with a focus on statistics
  • Good knowledge of statistical programming languages and tools including SAS and/or R
  • Knowledge in the conduct of integrated analyses, meta-analyses and network-meta-analyses as well as in epidemiology is advantageous 
  • Good communication skills and the ability to work both, independently and collaboratively
  • Ability to solve problems and to structure and simplify complex tasks
  • Fluent in English, both written and spoken

 

The position will be located in Wuppertal or Whippany.

.pre {white-space: pre-wrap;} Your application Are you looking for a new challenge where you can show your passion for innovation? Are you interested in working as part of a global team to improve people’s lives? Then send us your online application including cover letter, CV and references.

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