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(Junior) Clinical Data Specialist/eCRF Designer

  • Locatie:


  • Contactpersoon:

    Amandine Planche

  • Contractsoorten:

    Temp to Perm

  • Telefoon contactpersoon:

    +32 10 68 53 34

  • Bedrijfssectoren:

    Life Sciences, Clinical Research

  • E-mail contactpersoon:

Are you a motivated graduated Master/PhD in Sciences and you are eager to start your very first job in clinical research with many growth opportunities? Do you have an eye for detail, have a logical thinking and find teamplay important? Don't miss this opportunity!

Job Description

Every clinical trial needs its own application in order to collect all the data. Our client's EDC-team, which stands for Electronic Data Capturing, is the team that is responsible for designing, configuring and validating these applications.

You, as an e-CRF designer, will play a very important role in designing the data collection applications based on a clinical trial protocol and the pharma/biotech requirements. For this, you will receive extensive training during which you can enrich your scientific know-how with a flavor of computer programming.

You will also be responsible for the thorough follow-up of the data collection application. This means that you will ensure the review of the applications by working closely together with our pharma/biotech partners. You will incorporate relevant comments and implement changes when needed. Lastly, you will also configure/program the data validations rules based on the specifications.


  • Generate an (e-)CRF based on the clinical trial protocol and/or predefined specifications
  • Ensure review of the (e-)CRF by other parties (internal and external) until finalization
  • Incorporate relevant comments in the (e-)CRF
  • Implement changes to the (e-)CRF when needed
  • Generate and maintain the eDC tool Data Validation Rules based on the DVR specifications
  • Review the proof copy of the printer company in case of a paper CRF


  • You have obtained a Master's Degree in a paramedical area or biomedical sciences. A first experience in clinical research on your track record is a big plus, but not obligatory;
  • Your knowledge of English is very good, in written as well as spoken.
  • You are PC-minded!
  • You are eager to learn
  • You're a curious personality with a great eye for detail and quality minded
  • You are easy with words and possess excellent communications skills
  • You have a positive, constructive, professional attitude
  • You are stress-resistant, and you enjoy solving problems
  • You are able to set priorities and meet deadlines
  • You are a real team player?
  • You love to work in team and can handle stress like a pro, thanks to your well-organized competences.
  • Existing right to work in Europe is required


  • Fulltime position in a CRO
  • Long-term mission
  • Salary package with benefits

Vacancy number : 20784