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Senior CRA

Belgium   •  Permanent, Full time

My client, a full-service clinical contract research organization (CRO), are currently searching for an experienced CRA to join their team based in Belgium.

  • Conduct pre-study, initiation, monitoring, and closeout visits for research sites;
  • Perform source document verification and case report form review;
  • Perform regulatory document review;
  • Conduct study drug inventory;
  • Perform adverse event and serious adverse event reporting and follow-up; and
  • Assess patient recruitment and retention.


  • Minimum Bachelor of Science in health-related field; 
  • Previous experience as a CRA; with at least 2 years of experience;
  • Broad knowledge of medical terminology and clinical patient management;
  • Basic knowledge of drug therapy techniques and clinical research methodologies;
  • Broad knowledge of the local language (Dutch and French) and excellent English.

For further details, please contact Tim Barratt on +44(0)1727 817 626 or email tbarratt@achieva.co.uk

  • Agency: Achieva Group Limited
  • Reference: BH-34294
  • Posted: 19th January 2023
  • Expires: 16th February 2023

Achieva Group Limited

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