Experienced biostatistician

EORTC promotes cancer research in Europe and is linked to other leading biomedical research organizations around the world. EORTC research takes place in over 200 hospitals, universities and cancer centers in 32 countries and the unique network of investigators. The EORTC comprises more than 2000 clinicians collaborating.

The statistics department of EORTC is a team of approximately 20 analysts, fellows, statisticians, and epidemiologists, providing methodological support to the EORTC clinical trials and research projects. The department is at the forefront of methodological development through collaborations with several international initiatives and has a strong track  record in education in terms of methodological training in courses and workshops as well as in individual training through its fellowship program. This was acknowledged in 2015 when the department received the Flanders’ Training Network for Methodology and Statistics award (FLAMES award).

Main responsibilities

To take part in statistical activities relating to EORTC clinical trials and research projects, including but not limited to the following:

  • To provide methodological support for the development, conduct and reporting of clinical studies and exploratory research projects (development of the initial concept, writing the statistical sections of the protocol, supervising database setup and cleaning, writing the statistical analysis plan, preparing the statistical analysis reports and contributing to the publication of results).
  • To actively contribute to the development and maintenance of state of the art methodology in the department of statistics
  • To occasionally teach statistical methodology at training courses or conferences
  • To provide independent and objective methodological review of projects in line with internationally recognized guidance and practices.

Profile

The position is open for candidates with an MSc, PhD or ScD degree in biostatistics or statistics with at least 5 years of experience in clinical trials research in oncology. In addition, the position requires

  • Experience in the design of (preferably oncology) clinical trials and in survival analysis
  • Proficiency in the use of SAS; experience with R is an asset
  • Experience with CDISC/ADAM
  • Good communication skills in both oral and written English
  • Ability to work autonomously in an international multidisciplinary environment
  • Knowledge in health-related quality of life is an asset

Please send curriculum vitae and cover letter in English, and names of 2 referees.

Application form


*Compulsary fields
Application should be sent in English

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