Clinical Research Fellow
Drug Development Unit, Sarah Cannon Research UK
Main Purpose of this Post: To provide the highest standard of medical care for all patients participating in clinical trials. To be responsible for the daily management of patients as directed by the respective Consultant, ensuring that instructions are undertaken as directed. To ensure the Consultant(s) is informed of any changes in the patient’s condition whilst monitoring the patient in close liaison with the nursing staff. Only where immediate medical intervention is judged necessary should the Clinical Research Fellow take direct action before contacting the Consultant(s). The Clinical Research Fellow is expected to be competent in all aspects of cardio-pulmonary resuscitation and to have successfully completed the ALS course (in-house training offered, to be completed during the initial probation period). To maintain confidentiality as indicated by the Data Protection Act.