Clinical Trial Manager (Maternity Cover) x3 posts

About us

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. We are looking for individuals with good scientific and clinical trial acknowledge. The primary role of the post holder is to set up and support high quality clinical trials (across Phases 1-3) at the CCTU.

There are:

2 x 12 month roles and,

1 x 6 month role (with possible extension for a further 6 months).

These roles are all full time, fixed term maternity cover positions.

The post holder will report to the Clinical Project Manager.

Interviews will be held on 15 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.

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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