A key component of the post is to carry out the informed consent process with patients as appropriate and following specific training and administer the necessary paperwork and maintaining a clear audit trail. You will have responsibility for logging all patients into the EDGE research database and departmental clinical trials database ensuring information is accurate and up-to-date. Your role may also include some clinical skills such as taking clinical observations, venepuncture, cannulation, taking electrocardiography (ECG) tracings and processing clinical samples as agreed with manager and where appropriate with adequate documented training.
Report job
