Clinical Trial Practitioner

London Charing Cross Station, London (Greater)
£28,050 - £36,644, Full time, fixed term plus benefits
21 Feb 2019
06 Mar 2019
Contract Type

Job description Job summary

The Re-IMAGINE Consortium has been created to undertake discovery that will correct over-diagnosis, over-treatment, missed-diagnoses and poor risk-stratification in men with prostate cancer.

The project will combine the underlying molecular changes in the cancer with state-of-the-art imaging. This will allow the prediction of prostate cancer status for the individual (low, medium or high risk) without recourse to biopsy. It will also allow prediction of which prostate cancers are likely to progress over time and which are not, this has largely eluded scientist so far.

By doing so, men will be subject to fewer but better biopsies, improved risk stratification, appropriate treatment allocation, more benefit, less harm and more cost-effective care.

Re-IMAGINE will achieve this by building on established partnerships between patients, advocacy organisations, clinicians, imaging experts, molecular biologists, methodologists and a broad range of industrial partners.

The vision of Re-IMAGINE is built on recently published work showing that magnetic resonance imaging (MRI) of the prostate was 100% better at identifying men at risk compared to the standard prostate biopsy, and moreover missed no men with potentially fatal disease.

MRI is now certain to become the future cornerstone of the risk-stratification process for men at risk of early prostate cancer. However, little is known about the use of MRI in combination with other markers in the body. The Re-IMAGINE programme consists of a number of work-strands.

Duties and responsibilities

Establish a system to identify and recruit patients for clinical studies. Work as part of a team contributing to the screening, recruitment and consenting of patients along with the tissue and data collection for said patients in line with the deliverables of the Re-IMAGINE project.

The post holder will work under the direction of the Chief and Principal Investigators, the senior trial coordinator and the project manager to facilitate all processes associated with consenting, recruitment, retention, data collection and follow up of patients.

Essential requirements

The successful candidate will hold degree in a life science, registered nurse or other relevant medical or health care related qualification or equivalent. Proven clinical or management experience is essential in addition to previous experience of phlebotomy or willingness to complete training in phlebotomy.

Further information

This is a full time, fixed term post for 3 years. The post is due to start in June 2019.

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