Job Description

Clinical Research Associate | Brussels Area

Belgium Pharmaceuticals
Posted by Sarah on 08/04/2019

A new CRA function!
You will be responsible for the preparation, initiation, monitoring and closure within a certain number of clinical trials.
You will work in a BeNe structure.

Your profile :

  • University degree in related discipline, preferably in life science, or equivalent qualification
  • Minimum 2 years of experience in a CRA-function
  • Excellent knowledge of international guidelines ICH/GCP
  • Already know-how with oncology is a big plus
  • Fluent in Dutch, French and English

The description:

  • Maintain essential documentation in compliance with ICH-GCP
  • Participate to the selection of potential investigators, train, support and advise Investigators and site staff in study related matters
  • Initiate, monitor and close study sites
  • Prepare for activities associated with audits and regulatory inspections
  • Work with sites and data management

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