About the role
This office based role,will be responsible for the day-to-day co-ordination, trial and projectmanagement of their clinical studies, working with the other members of theteam and sites to ensure the safe and successful delivery of the study. Themain duties of the post include writing and managing documentation, setting upand assisting sites upload images to XNAT, training the site staff on the studyprocedures, designing MACRO databases, managing the data and ensuring that allregulatory and other relevant requirements are met in a timely manner. Theapplicant should have relevant skills, abilities and experience to conductthese roles or the aptitude to learn these on the job.
About you
The candidate must have experience of running clinical trials, and with working with XNAT and MACRO. The role is office based, the applicant will need to be a flexible worker, have good organisational skills. The individual needs to enjoy being part of a team, with a good eye for detail. And have good communication skills both written and verbal.
What we offer
This is an exciting opportunity to join a multidisciplinary team working across the Division of Medicine. As well as the exciting opportunities this role presents, we also offer some great benefits some of which are below: • 41 Days holiday (27 days annual leave 8 bank holiday and 6 closure days) • Additional 5 days’ annual leave purchase scheme • Defined benefit career average revalued earnings pension scheme (CARE) • Cycle to work scheme and season ticket loan • Immigration loan • Relocation scheme for certain posts • On-Site nursery • On-site gym • Enhanced maternity, paternity and adoption pay • Employee assistance programme: Staff Support Service • Discounted medical insurance