Support for your research team can be found at KCL https://www.kcl.ac.uk/research/support/professional-development
Staff can be notified of KCTU training events
Changes to planned protocol
https://www.myresearchproject.org.uk/help/hlpamendments.aspx
Study site monitoring for adherence to protocol, data quality and safety reporting via on site and/or remote monitoring and/or central data cleaning activities are crucial for the success of the trial and processes should be discussed and agreed in the context of Trial Management Group meetings
If the study has problems with budgets, timelines, recruitment targets or data quality, the issues should be discussed in a Trial Management Group meeting and escalated where appropriate to the independent oversight committee and/or sponsor and/or funder.
If your study is in the area of mental health or neurosciences, please make an appointment initially to speak to an NIHR RSS advisor at www.ctu.co.uk/NIHR-RSS
For all other clinical areas, a brief support request form must be submitted.
We strongly advise that researchers approach KCTU at the grant application stage, ideally 3-4 months in advance of the submission deadline to get the best possible input and consideration.
Requests for support are circulated to the relevant senior academic and operational staff for consideration, to ensure that the best possible match between the trial and the expert collaborator is achieved.
020 7848 0532 | ctu@kcl.ac.uk
Clinical Trials Unit
King’s College London PO64, Room M2.06,
Institute of Psychiatry, 16 De Crespigny Park,
London, SE5 8AF
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