Data 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 standard.

About the role

We currently have vacancies to work within the unit, which is based in Holborn, London.

We have two roles available:

• 1 x full time permanent role
• 1 x 0.6 FTE permanent role

The post holder will report to the Trial Manager.

Interviews will be held on 22 July 2024 at 90 High Holborn.

A job description and person specification is available at the bottom of the page. Please provide your CV and a cover letter explaining how your skills and experience are applicable to the role. Please specify which role you are applying for in your cover letter.

About you

An enthusiastic individual is sought for this post which is based on the Bloomsbury campus in London. The primary role of the post holder is to assist with the efficient collection, processing, validation, and quality assurance of data from trials.

The successful applicant will have experience of data entry and data management, excellent communication skills and experience of working on a clinical trial or in a medical research environment. Experience of word processing, using Microsoft Word, Excel and Access are also essential requirements for this post.

The role holder will be responsible to the Trial Manager and the post is full time and funded for one year in the first instance.

Please note that we are unable to support visa sponsorship for this role. A job description and person specification can be accessed at the bottom of this page.

If you have any queries regarding the vacancy please contact Felicia Ikeji - .

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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