Clinical Trial Manager - Comprehensive Clinical Trials Unit

About us

The UCL Institute of Clinical Trials and Methodology
The Institute was established on 1 August 2013 and is formally comprised of two Research Departments: The MRC Clinical Trials Unit at UCL (MRC CTU) and the Comprehensive Clinical Trials Unit at UCL (CCTU). It currently directly employs 265 staff and generates an annual income in excess of £30 million. Over time and building on the strengths of its Research Departments the mission of the Institute is to become a centre of excellence for the conduct of all phases of clinical trials, meta-analysis and epidemiological studies. Key areas of focus for the Institute will include delivering innovations in trial methodology, training and developing the next generation of trialists.

Comprehensive Clinical Trials Unit (CCTU)
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 led by UCL Chief Investigators. The CCTU provides clinical, statistical and trial operations and facilitates the delivery of high quality, regulatory compliant clinical trials of investigational medicinal products (IMPs) and non-IMP trials. The CCTU is a registered CTU with the capability to centrally coordinate multi-centre clinical trials (i.e. having overall responsibility for the design, development, recruitment, data management and analysis of trials) with robust systems to ensure conduct and delivery of clinical trials to the highest quality standards.

About the role

We currently have vacancies to work within the unit, which is based in Holborn, London. The primary role of the post holder is to set up and support high quality clinical trials (across Phases 1-3) at the CCTU.

This role is a full time, permanent position.

The post holder will report to the Clinical Project Manager.

Interviews will be held on 15 July 2024 at 90 High Holborn.

Please provide your CV and a cover letter explaining how your skills and experience are applicable to the role.

About you

An enthusiastic, committed and professional individual.

The successful applicant must possess a degree and/or equivalent experience in Clinical Trials, as well as recent experience in the coordination of clinical trials involving Investigational Medicinal Products, a comprehensive understanding of UK Clinical Trials Regulations, the European Directives on Clinical Trials and Good Clinical Practice and the Department of Health’s Research Governance Framework.

We are looking for someone with good scientific and clinical trial acknowledge. An ideal candidate would possess on-site monitoring experience, good communication skills, an ability to work within a multi-disciplinary team, experience of study trial documentation development, excellent attention to detail and organisational skills and a willingness to travel within the UK and/or internationally. Previously experience working in neurology, rheumatology and paediatric trials would be advantageous.

An experience of Line Management would be advantageous, however is not essential.

If you have any queries regarding the vacancy please contact Felicia Ikeji or James Blackstone.

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.

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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