An experienced administrator is sought to contribute to a dynamic and supportive academic environment within one of the leading cancer clinical trials units, the ICR's Clinical Trials and Statistics Unit (ICR-CTSU)
ICR-CTSU runs a diverse portfolio of national and international phase III multicentre randomised controlled trials, and phase II trials of targeted treatments with a focus on breast, urological and head and neck cancer treatments.
The successful applicant will work within the Research Administration Team to support the efficient running of ICR-CTSU.
Key responsibilities include:
1. general office administration
2. ensuring recruitment administration runs smoothly
3. arranging training and tracking compliance
4. setting up and maintaining robust filing systems and records in accordance with regulatory requirements for clinical trials
5. supporting the maintenance of quality management systems.
Key Requirements
You should be numerate and possess strong communication and problem-solving skills to be successful in this role. A broad range of administrative experience is essential, including maintaining filing systems, using advanced level IT skills and organising and prioritising a varied workload. Experience documenting working practices (e.g., process notes/SOPs) would be an advantage.
We encourage all applicants to review the attached job pack for full details about this role. When applying please include a supporting statement outlining your reasons for applying and demonstrating how your experience meets the requirements for the post.
Further details
This is an office-based role. Requests for hybrid working (splitting time between our Sutton site and home) may be considered following successful completion of key training and only if the role allows. Flexible working options may also be considered.
Informal enquiries may be made by emailing ctsu@icr.ac.uk