Clinical Trial Coordinator - Charing Cross, United Kingdom - Imperial College London

Imperial College London

Verified Company

Charing Cross, United Kingdom

1 week ago

Posted by:

Tom O´Connor

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Description

The Imperial jobs site will be temporarily unavailable from 16.00pm Friday 23rd February to 12.00pm Wednesday 28th February as we move to a new Job site platform.

Applications started, not yet submitted by 16:00 23rd February will need to be started again on the new platform.

An exciting opportunity has arisen for the appointment of a Clinical Trial Coordinator to work on a randomised controlled trial investigating a neuromuscular electrical stimulation device in people with diabetes experiencing diabetes-related nerve damage (diabetic neuropathy).

The post holder will assist with day-to-day coordination of the study, patient screening, recruitment and follow-up, conducting trial assessments and collecting and entering trial data.

Duties and responsibilities:

Day-to-day coordination of the randomised controlled trialPerform pre-screening calls with potential participantsScreen, recruit, follow-up and liaise with participants

Arrange patients for the study visits and book their nerve conduction studies and blood tests, travel when required, and ensure their comfort and provide refreshments/subsistence when necessary
Perform trial assessments of the participants, this includes nerve function tests and questionnaires Collect receipts and arranging payments for participants
Coordinate, maintain data and documentation to a sufficient standard and to ensure the smooth running of the trial
Work closely with the Chief Investigator, Principal Investigators, Clinical Trial Manager, Clinical Trial Monitor, Study Funder and other collaborators to establish and maintain good communication between all parties

Essential requirements:

First degree or equivalent in a biomedical/scientific or allied field
Experience of working within the NHS or an academic clinical research setting
Experience in patient screening or recruitment or follow up
Experience in performing study assessments
Experience of data collection and entry
Knowledge of data capture and storage systems (e.g. REDCap)
Knowledge of clinical trials and their associated regulations (e.g. EU Clinical Trials Directive/The Medicines For Human Use Regulations, GCP, GDPR, Research Governance Framework, Human Tissue Authority).

Further information:

This part-time position (80%FTE, approximately 28 hours a week) is offered for a fixed term of 12 months with the possibility of extension based at the Section of Vascular Surgery in Charing Cross Hospital (Hammersmith, London).

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