About the role
The post holder will be responsible for coordinating clinical trials, and ensuring the efficient and safe management of these trials with adherence to the study protocols, current regulatory requirements and UK legislation. A crucial aspect of this will be close liaison with participating institutions.
The post holder will be supported by a Senior Project Manager and will be responsible for the day-to-day coordination and data management of multiple trials.
The CTC offers hybrid working with staff being able to work flexibly between our office and home, along with core hours and flexible start/finish times. It is expected that the post holder would work onsite for a minimum of 60% of their time (3 days per week for full time staff).
This is a full-time, open-ended post with funding for 1 year in the first instance. Appointments are usually made at the beginning of the salary scale.
This is a re-advertisement - previous applicants need not apply.
About you
The post holder will have a high level knowledge of biomedical sciences and experience of clinical trials (preferably within a clinical trials unit) and/or health related research.
What we offer
As well as the exciting opportunities this role presents, we also offer great benefits. Please visit to find out more.