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Job Details

Clinical Research Associate (CRA) - Belgium

Company: RBW Consulting
Location: Belgium
Reference: DH1410
Closing Date: 14 Nov 16
Type: Full Time
Salary (£): On Application
Benefits: Excellent, Full Benefits on Application

Job Summary:

CRA position in Belguim for a global organisation.


The Company

The company offer a diversified insight into the world of clinical research. The successful candidate can expect to work with a highly-qualified and dynamic team who will help strengthen your scientific profile. You can also look forward to a flexible working environment and a pleasant atmosphere. Due to this position being client-facing my client need a confident individual to work independently and create a strong relationship with the client.


Necessary Experience

  • Educated to degree level (health related discipline)
  • Minimum of 2 years independent monitoring experience in clinical research
  • Competent in written and oral English


Ideal Candidate

  • Experience of CTMS
  • Strong understanding of EDC systems and IVRS 



  • Perform all clinical monitoring/site management activities for assigned projects in accordance with the company's standard operating procedures
  • Act as the company's direct contact with assigned clinical sites, and use judgment to assess and ensure overall integrity of study implementation, as well as adherence to study protocol
  • Conduct qualification visits (QV), site initiation visits (SIV) and monitoring visits (MV) at assigned clinical sites
  • Good knowledge of applicable clinical research regulatory requirements such as: Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Function as a mentor and role model for other CRA team members
  • Arranging on-site visits and logistics
  • Establishing a site recruitment plan in collaboration with site staff during QV
  • Monitoring completeness and quality of Regulatory Documentation
  • Performing site documentation verification
  • Collecting data and drug accountability in accordance with ICH GCP guideline
  • Monitoring patient safety on-site and addressing any violations in a timely manner

Please contact me for further details.

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At RBW Consulting LLP, every one of our consultants has the benefit of five years experience in helping Pharmaceutical Professionals find the jobs they are looking for in the industry.

With unrivalled industry knowledge and excellent links with hiring managers in Biotechs, Pharmas and CROs throughout the UK, Europe and across the world, we would be delighted to speak with you about the role you are looking for. Call +44 (0)1293 584 300 or email for a confidential discussion about your options for progression.

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Apply for this job: Clinical Research Associate (CRA) - Belgium

Contact Information:

Address:  Head Office
Origin Two 106 High Street, Crawley RH10 1BF
RH10 1BF
Tel:  01293 584 300
Fax:  01293 534 133
Website:  Visit Our Web Site

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