Key accountabilities

As a clinical data manager you will manage the processing of clinical trial data from reception until the data is ready for statistical analysis. You will execute activities to ensure completeness and of the data. This process consists of

  • setting up the clinical database
  • code data (coding of medication)
  • performs verifications in order to have consistent data
  • Integrate external data
  • Define protocol deviations
  • Operate in line with the standard operating procedures
  • Take ownership of quality, timelines and budget aspects related to Data Management for your clinical studies
  • Coaching and mentoring less experienced Data Managers, and providing internal training to regarding Data Management.

You will be part of a multidisciplinary team that is focused on getting qualitative data that meet international standards.

Key competencies

  • Eye for detail
  • Achievement oriented
  • Team spirit
  • Customer focus
  • Integrity and trustworthy

Key requirement

This position requires:


  • A health or science related Master Degree Experience
  • Minimum 5 years of experience with conduct of clinical trials

Skills/Know How

  • Excellent Verbal and written skills in English as well as Dutch or French
  • Knowledge of SAS®
  • Knowledge ofMedDRA / WHO Drug dictionnary

We offer the opportunity to develop personally and professionally within a growing company, flexible work conditions and a competitive compensation package.


Send your application to:

DICE - Koning Albert Avenue 160, B-1082 Brussels

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