The role of the Chief Investigator

For multi-centre trials there will be a designated Chief Investigator or lead Clinician. Prior to commencement of a trial, the Chief Investigator is responsible for preparation of the protocol. During the conduct of the study he/she is in charge of medical monitoring (particularly toxicity/safety) and, finally, on completion of the study he is responsible for liaison with statistican over analysis, and finally for reporting the results.

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