This three hour course is for experienced research delivery staff who have already done GCP training, have recent practical experience of working in a clinical research environment and have a good understanding of the principles and quality standards of GCP and related frameworks. More information

Tuesday 12 November 11:00 -12:30 Seminar Meeting Room, Boundary Brook House Thursday 12 December 11:00 -12:30 Seminar Meeting Room, Boundary Brook House So, you’ve got a great idea for a research study - but what approvals do you need before you can start? Who do you apply to? And how do you go about doing... READ MORE

For anyone involved in grant submissions or the set up and co-ordination of clinical trials. This workshop aims to increase your understanding of the basic principles of cost attribution for clinical research studies within the NHS in line with AcoRD guidance. More information

This one day workshop is designed to provide participants with an insight into the necessary communication skills needed to receive true valid informed consent from trial participants. More information

Basic laboratory skills are essential to ensure confident and competent handling of study supplies and equipment, enabling research staff to contribute to the delivery of clinical research protocols as part of their research team. More information

This half-day workshop is designed to provide the opportunity to explore the consent process in more depth and covering the requirements for NIHR portfolio studies and clinical trials conducted within the NHS. https://local.nihr.ac.uk/events/thames-valley-and-south-midlands-valid-informed-consent/14136