Clinical Research Associate - all

Role:

Clinical research Assoc

Clinical Research Associates – All Levels - UK

In partnership with its client CPL are currently seeking several Clinical Research Associates for a permanent roles based in a Clinical Research Organisation in the UK.

The Client:

My client is a leading Clinical Research Organisation, with a global presence. This position is based in the UK.

Fluent English is essential for this position. Additional language skills would be a benefit.

Job Requirements

Working within a highly qualified team you will identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV ensuring that applicable regulations and principles of ICG-GCP are adhered to.

Job Responsibilities

With a University degree in medicine, science, or equivalent, you will have previous monitoring experience in medium sized studies including study start up and close out (for all roles above Entry Level).  In addition, you will also require:

•  You will have knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
• Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner
• Ability to produce accurate work to tight deadlines within a pressurised environment
• Computer literate with Microsoft Office
• Must be available to travel international and domestic (at least 60% fly and drive) and should possess a valid driving licence.
• Ensure that relevant new contracts / cost proposals are reviewed in order to enable the preparation of audit plans.

•  1 - 2 years monitoring experience within the UK would be highly beneficial.
  
• All therapeutic disciplines will be considered

All applications will be treated with the strictest of confidence

CPL Contact:

To apply or for further information please contact Jenny Navan on +353 1 614 6072 or e-mail with you updated CV to jenny.navan@cpl.ie

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