Do you want to be part of an established Quality Assurance (QA) team with an aim to improve clinical trial research within Leeds? Are you an enthusiastic and driven individual with working knowledge of Clinical Trials and Good Clinical Practice? Are you interested in using your knowledge, skills and experience to support research delivery across Leeds Teaching Hospitals Trust / University of Leeds? Do you enjoy meeting new people and leading discussions?
The University of Leeds (UoL) and Leeds Teaching Hospitals NHS Trust (LTHT) regularly Sponsor in house Clinical Trials of an Investigational Medicinal Products (CTIMPs) and are responsible for their management in line with the Medicines for Human Use Clinical Trials Regulations.
The joint UoL and LTHT QA function provides guidance and a common framework for researchers for regulatory compliance across both organisations. You will join the team as a Clinical Trials Monitor, responsible for monitoring a portfolio of LTHT and UoL Sponsored CTIMPs against Good Clinical Practice standards and the Clinical Trial Regulations. This will include leading site visits within LTHT and performing central monitoring from within the QA office.
You will regularly be required to meet new people and lead multi-disciplinary meetings with a training focus. You will have experience of working in a quality-assured clinical research environment, including experience of Phase II / III trials and will have a current working knowledge of applicable legal and ethical frameworks.
Attention to detail, organisational, interpersonal and communication skills (including written and presentational skills) plus an understanding of key issues pertaining to clinical research are essential.
To explore the post further or for any queries you may have, please contact:
Stephanie Britt, QA Regulatory and Governance Affairs Officer
Tel: +44 (0)113 20 60464, email: stephanie.britt@nhs.net or s.l.britt@leeds.ac.uk
Closing Date: 31 Mar 2019
Category: Administrative and Clerical Support
