Descrizione:
This is an exciting opportunity with candidates to start and interview as soon as possible!
The Clinical Study Coordinator must have minimum 1/2 years' clinical research experience as they need an individual who can work independently as well as part of a team. Day to day responsibilities will involve will support maintenance of study files, lab kits and study supplies, ordering lab kits, shipping samples, booking procedures and scheduling subject visits and preparing the site for monitoring visits.
Il trattamento dei dati personali pervenuti si svolgera' in conformita' alle normative vigenti.