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Clinical Research Associate, Netherlands

Belgium   •  €0 per annum  •  Permanent, Full time


(please note, the salary for this role willl depend on your level of experience)
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 i
  • 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 excellent English

About the client:
Within this role, you will be working for a full-service clinical contract research organization (CRO), providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Their mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. They leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 4,000 people across almost 40 countries.

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-32754
  • Posted: 10th May 2022
  • Expires: 7th June 2022

Achieva Group Limited

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