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We currently have a permanent position for a Clinical Research Associate, based in Middlesex or Surrey depending on the candidate’s preference. You will be responsible for co-ordinating required study activities for an international CRO as required by the client. You should have a good working knowledge of, and be able to assure compliance with the ICH and FDA Good Clinical Practices, applicable regulatory and legal requirements, and company (or client, according to exhibit) Standard Operating Procedures. You should have a degree or equivalent in life sciences, and have at least one years experience as a CRA. This position will involve travel around 3 days per week, and as such you should be flexible, and be open to overnight stays.
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