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Job Details

CRA, Clinical monitoring

Company: RBW Consulting
Reference: MK/CRA8103
Closing Date: 01 Mar 18
Type: Contract
Salary (£): On Application

Job Summary:

CRA, Senior CRA, Lead CRA, Clinical Research Associate, Monitor, Monitoring, International Monitoring, Senior Monitor


A leading global CRO has had an opportunity arise for a candidate with strong communicational and organisational skills to join their experienced and dynamic Clinical team as a Clinical Research Associate.  This exciting opportunity has arisen due to the continued growth within the company this last year and is already set for a great 2018.

As a Clinical Research Associate your responsibilities will be to:

  • Maintain GCP documentation for assigned trial sites within the scope of the trial contract
  • Support  the Clinical Study Manager by assessing the project feasibility and undertaking site selection and recruitment
  • Collaborate with other departments and report trial site status
  • Perform monitoring visits and source data verification as contracted ensuring the delivery of high quality data from sites within given timelines
  • Understand the ISO guidelines and work within all GCPs whilst maintaining a working knowledge of applicable SOPs


The ideal candidate will have a minimum of two years’ experience working as a Clinical Research Associate and will also be a driven individual, keen to motivate others and have strong communication and interpersonal skills.  In return you can expect to join a team that offers you all the tools that you would ever need to enable you to learn new skills and progress your career along the right path.

To find out more about this fantastic opportunity contact Marème Kaloga on +44 (0) 1293 584 300 and send your CV through to

Apply for this job: CRA, Clinical monitoring

Contact Information:

Address:  RBW Consulting LLP, Crawley, Zug Branch
Grabenstrasse 42, 6301 Zug, Switzerland

Tel:  0800896891
Website:  Visit Our Web Site

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