The post holder will be responsible for managing their own cohort of clinical trials including set-up, maintenance and closedown of trials and co-ordinate the management of the Investigational Medicinal Products in all pharmacy trials. They will be responsible for ensuring compliance with current legislation, the international ethical and scientific quality standard laid down in The International Conference on Harmonisation guidelines for Good Clinical Practice relating to trials (ICH GCP) and The EU Clinical trials directive (2001/20/EC) as transposed into UK law by the Medicines for Human Use (Clinical Trials ) Regulations 2004 (the legislation), and any other legislation or standards for the conduct of clinical trials (including maintaining records, writing and reviewing SOPs and training).