Clinical Study Unit Safety Assistant
45 minuuten geleden

Job Overview

Join Covance and our FSPx Department!

We are actively recruiting a Clinical Study Unit Safety Assistant to join the team of one of our client based in Brussels.

As part of this role, you will be involved in Pharmacovigilance and Safety tasks related to clinical studies and programs in humans.

This is an exciting opportunity to grow in a dynamic and motivating environment where team work is valued.

Responsibilities :

  • Provide assistance to the Clinical Study Unit Safety Lead in defined Pharmacovigilance tasks and safety documentation
  • Reporting of safety events according to Local Regulations and Corporate and Local Quality Documents
  • Ensure that minimum criteria for received cases are completed, supporting documents
  • translated into English (if applicable), and forwarded to GPV, in a timely manner

  • Review AE and contact CRA (if available / necessary)
  • Send case information to GPV
  • Reception of acknowledgement of receipt
  • Files electronically
  • SUSAR Management for BE / NL / UK / Lux / Ireland
  • SASR / DSUR Management for BE / NL / UK / Lux / Ireland
  • When joining Covance you will be :

  • Welcome in a supportive team environment
  • Receive on-the-job training and mentoring if needed or be a mentor to others
  • Enjoy the benefits of working for a company that values a WORK / LIFE BALANCE
  • Education / Qualifications

  • Professional bachelor or equal by experience
  • Fluency in French, Dutch and English
  • Professional experience : professional experience in Drug Safety,
  • Clinical Development or Clinical Research is an advantage


  • Experience working in clinical studies (eg. Previous CPA, CRA experience or similar)
  • Professional experience in Drug Safety Development or Clinical Research is an advantage
  • If you are interested in knowing more about Covance and this thrilling opportunity, contact Recruiter Christelle.segabiot

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