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VC437028 SVDL

Via Brunel

Published on 18 days ago

Do you have expercience with clinical trial biostatistics and looking for a new challenge?

Check out this vacancy!


Job description

  • The services on this assignment will be in support of existing project teams, planning, interpreting and the results on late stage clinical trials


  • MSc or PhD in Statistics.
  • Multiple years (preferably minimum 5 years) of relevant clinical trial biostatistics support in design, analysis and interpretation. Proven experience of work with clinical trial data in support of safety and efficacy analysis.
  • Knowledge and strong experience in survival analysis, linear and generalized linear models.
  • Capacity to interface effectively with clinicians and statistical programmers.
  • Capacity to work independently or under the guidance of a senior MSD statistician.
  • Capacity to quickly read late development protocols, to understand the statistical methodology and to apply to clinical data.
  • Knowledge and practice of CDISC SDTM and ADaM data standards.
  • Ability to work complying to the company Analysis and Reporting SOPs and project data standards. 
  • Fast learner, team oriented, able to work independently.
  • Ability to read, write and speak fluently in English.
  • Knowledge of SAS programming SAS/STAT SAS/BASE, SAS macro language. Experience with SAS on PC and UNIX platforms.


  • An interesting salary package
  • A dynamic and high-tech life sciences environment

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Blarenberglaan 3, 2800 Mechelen

Grotere kaart weergeven
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42 days left to apply



  • Professional bachelor (Higher Education Short Type)
  • At least 5 years experience
  • English


  • Permanent
  • Full-time

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