Clinical Trial Administrator

YOUR RESPONSIBILITIES WHAT YOULL DO The role involves collation of data for clinical trial activities performed in each study and creating invoices accordingly, creating credit notes as necessary and organising monitoring and close out visits as required by the trial sponsor. The post holder will also be involved in liaising with oncology/haematology staff over patient identification and treatment schedule, prescription requirements; ensuring sufficient IMP supplies are available as well as processing of deliveries. WHAT WERE LOOKING FORPost holder must be numerate and literate, with good keyboard skills and a working knowledge of computer software packages. Candidate should possess a professional attitude to their work and have the ability to work flexibly in a busy environment. Ideally candidate will have proven experience within a clinical trials or an office environment. Will be required to work as part of a team as well as being, able to use their initiative and prioritise their

workload to meet deadlines, We welcome interested applicants to contact the department for more information or an informal visit. Please contact CTA Team on or Liliana Cordeiro, Head of Clinical Trials Pharmacy on .