For further information on this role, please see the attached detailed Job Description and Person Specification: To maintain full working knowledge of the in-house software used to collect and analyse clinical research data. To maintain knowledge of the EU directive on clinical trials (EU directive 2001/20/EC) and ICH GCP according to EU directive 2005/28/EC. To gain a good knowledge of the clinical features, management and treatment of the disease being studied, and to keep abreast of developments. To gain a working knowledge of the RMH EPR in order to liaise with users and analyse data where necessary. To liaise with, advise and educate clinicians on the design aspects of clinical trials, research studies and audits and to be responsible for the statistical design where appropriate.