Training & development

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TRAINING CONSULTATION 

The Health Research Authority (HRA) and Medicines for Healthcare Regulatory Agency (MHRA)
published a Joint Statement paper outlining the requirements for researcher training in October
2017. https://www.hra.nhs.uk/about-us/news-updates/updated-guidance-good-clinical-practicegcp-training/

The publication is designed to help establish a pragmatic and proportionate approach to researcher training and aims to reduce the burden of unnecessary training for the research community.

In light of the content of the joint statement, University Hospitals of Leicester NHS Trust (UHL) and the University of Leicester (UoL) through the Joint Office for Research in Healthcare wish to seek opinion on proposed changes to the requirements for researcher training.

FULL DOCUMENT: Researcher Training Consultation v3

Please complete the Survey Monkey survey https://www.surveymonkey.co.uk/r/SGNTCP2 by Friday 21 December 2017.

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Welcome to the training and development section of this website managed by the Clinical Trials Monitoring and Training team.

As part of the on-going support provided to researchers by the Research and Innovation department, the training team provides Good Clinical Practice for CTIMP Studies training, Research Training for Non CTIMP studies, Informed Consent Training and Site File Management training for studies sponsored or hosted by Leicester’s Hospitals.

Training is run on a monthly basis. Access the calendar to view the sessions available. Bookings can be made via email at RITraining@uhl-tr.nhs.uk.

The training team provides training and support to research teams. We have an in depth knowledge and understanding of working within the research field, drawing on the team’s varied research expertise.

Leicester’s Hospitals’ requirements for training are set out in the following Standard Operating Procedures (SOPs):

SOP S-1008 UHL Training for staff in SPONSORED research

SOP C-2005 UHL Training for staff in HOSTED research

The following courses are currently offered by the training team (click on links for further details):

Good Clinical Practice (GCP) for Clinical Trials involving Investigational Medicinal Products

Good Clinical Practice for non-CTIMP Studies

Informed Consent for Research Studies

Site File Management Training

External training providers

Additional GCP training is offered by external providers. Please click on the links below or view the calendar for dates and locations of their training.

NIHR CRN: East Midlands

University of Leicester (Research training for Non CTIMP studies – principles of GCP)

For dates of all events, please see the calendar below: