DUTIES

• Establish  workflows  with  the departments  and  staff  identified as  collaborators  in  the  assigned clinical trial.
• Involvement in the enrolment of new patients in assigned clinical trials: reviewing, together with the principal investigator, the inclusion criteria and the tests required by the protocol.
• To participate in the reporting of serious adverse events occurring in a clinical trial, in accordance with current legislation and the sponsor’s requirements, following review and signature by the investigator.
• To help address any queries patients may have before and during their participation in the study.
• Attend the Unit’s clinical sessions, regular clinical research sessions and any training sessions required by the Head of Clinical Operations at the UEC.
• To organise and take part in, in consultation with the principal investigator, the closing visit of the clinical trial, liaising with the Head of Clinical Operations at the UEC to ensure the trial records are stored for the period required by current legislation.