Co-ordinating and setting up in-patient and outpatient clinical research studies: Assist with the submissions of studies to the required review bodies. Responding to correspondence to obtain approval, and reporting all changes and unanticipated problems involving patient care Assembling, completing and maintaining the required regulatory documentation Ensure that the study is conducted adhering to the International Conference for Harmonisation (ICH) and Good Clinical Practise (GCP) guidelines, UK Clinical Trials Regulations and in accordance with its protocol Attend Investigator meetings and set up meetings Identify and screen for potential research participants Be able to advise and support patients and their families when considering participation in a study Teach, advise and support medical and nursing staff about the studies so that they can identify, recruit, administer study drugs and care for study patients according to the specific protocol requirements Ensure availability of clear and easy to follow study guidelines, so that staff workload is kept to a minimum For further information please refer to the .
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