You will be expected to work flexibly as part of a team to provide administrative support to the trials, the clinical trial managers and the Unit. You will work closely with the trial team, trial managers, senior trial manager, investigators, site staff and R&D departments to support the successful completion of studies. 

Duties will include printing and sending out materials to study sites and pharmacy; maintenance of Trial Master Files and local site files; planning travel arrangements and meetings; data entry and raising data queries. 

Candidates must have a minimum of GCSEs (or equivalent) in English and mathematics (Grade A-C) or relevant vocational qualifications (eg NVQ 2/3 administration, City and Guilds) or equivalent, plus some experience in a relevant role. Candidates should have good organisational skills, a high level of IT skills, capable of working without close supervision, show ability to plan and prioritise work activities with good attention to detail and the ability to work flexibly as part of a team as well as individually; and a good telephone manner. Knowledge of databases and experience of working within a busy healthcare or research environment is desirable. 

The post is offered on a fixed-term contract for a period of one year. Hours of work are full-time (36.25 hours per week) ; however applications are also welcome from candidates wishing to work part-time (minimum 29 hours per week). Please specify in your application if you wish to work part time and the number of preferred hours. Job share arrangements may be considered. 

Requests for secondment from internal candidates may be considered on the basis that prior agreement has been sought from both your current line manager and the manager of your substantive post, if you are already undertaking a secondment role. 

This role can be fully office-based or open to a hybrid working model with a blended approach of home and office working. Typically, you will work a minimum of 2-3 days (pro-rata) per week on campus.