Quality Assurance Manager
UCL - Comprehensive Clinical Trials Unit (CCTU)
| Location: | London, Hybrid |
|---|---|
| Salary: | £52,487 to £61,534 |
| Hours: | Full Time |
| Contract Type: | Fixed-Term/Contract |
| Placed On: | 19th November 2024 |
|---|---|
| Closes: | 3rd December 2024 |
| Job Ref: | B02-07969 |
About us
The Comprehensive Clinical Trials Unit is a specialist unit set up within the Institute of Clinical Trials and Methodology with a specific remit to design, conduct, analyse and publish clinical trials and other well-designed studies. The Comprehensive CTU is a registered CTU that provides clinical, statistical and trial operations and facilitates the delivery of high quality, clinical trials of both investigational medicinal products (IMPs) and non IMPs.
About the role
An enthusiastic, committed and professional individual is sought for the role of Quality Assurance Manager, which is based on the Bloomsbury campus, London. The main purpose of this post is to ensure that staff at the CCTU conduct clinical trials in accordance with applicable guidelines and regulations. In particular the role holder is responsible for maintaining and overseeing Quality Management Systems at the CCTU, including the portfolio of central standard operating procedures (SOPs), providing/arranging staff training relating to the procedures and conducting a programme of internal audits. The position involves liaison with all staff at the CCTU and with a wide range of academic, managerial and administrative staff, including the Joint Research Office, the Institute of Clinical Trials and Methodology and other departments within UCL. Contact with regulatory bodies and research ethics committees regarding QA and auditing issues is also essential to the role.
Interviews will take place on 12 December 2024.
If you have any queries regarding the vacancy or the application process, to arrange an informal discussion regarding the post please contact us.
About you
The successful applicant must possess a postgraduate degree and/or equivalent experience in Clinical Trials, as well as a comprehensive understanding of UK Clinical Trials Regulations, ICH Good Clinical Practice, the European Directives on Clinical Trials and Good Clinical Practice and the Department of Health’s Research Governance Framework. Experience of working in a clinical trial regulatory environment is also required. Experience of staff supervision or line management would be required for this post as well as experience of establishing and maintaining quality management systems.
What we offer
As well as the exciting opportunities this role presents, we also offer great benefits. Please visit https://www.ucl.ac.uk/work-at-ucl/rewards-and-benefits to find out more.
Further information about the Institute is available via the Institute website.
Our commitment to Equality, Diversity and Inclusion
You can read more about our commitment to Equality, Diversity and Inclusion here: https://www.ucl.ac.uk/equality-diversity-inclusion/
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