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eCRF Designer

Jumpstart your clinical research career with this great opportunity!

Job Description

The main tasks of the eCRF Designer 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 eCRF Designer 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 are a curious personality with a great eye for detail and quality minded;
  • You 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.

Benefits

  • A balanced salary package based on your capabilities and experience, including meal vouchers,...
  • A full time position
  • Temporary assignment, with option fixed after 4 months

Existing right to work in Europe required ( please read job spec in full before applying ).

Vacancy number: 17883