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Senior CRA

Netherlands   •  Permanent, Full time


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

  • 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.

 
Qualifications:

  • Bachelor of Science in health-related field
  • Previous experience as a CRA
  • Broad knowledge of medical terminology and clinical patient management
  • Basic knowledge of drug therapy techniques and clinical research methodologies; an
  • Broad knowledge of the local language (Dutch) 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-34293
  • Posted: 19th January 2023
  • Expires: 16th February 2023

Achieva Group Limited

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