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e-CRF Designer

  • Location:

    Mechelen

  • Contact:

    Santina Fourneaux

  • Job type:

    Temp to Perm

  • Industry:

    Pharmaceutical

  • Contact email:

    santina_fourneaux@oxfordcorp.com

For one of our clients we are looking for a e-CRF Designer.

Job Description

The main tasks of the (e-)CRF Designer ((e-)CRF-D) consist of designing data collection tools (DCT) (e-CRFs or paper CRFs) based on a clinical trial protocol and the sponsor's requirements and specifications. The (e-)CRF-D is also responsible for the thorough follow-up of the data collection tool.


Responsibilities

  • 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


Requirements

  • 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 and Dutch 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;
  • What's a team without a team player?
  • You love to work in team and can handle stress like a pro, thanks to your well-organized competences.