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With appropriate support you will manage, co-ordinate and implement the PICNIC study across 3 UK sites, liaising with the study sponsor, local R&D colleagues and project management teams to conduct and deliver a safe, high-quality study. You will provide support to more junior team members within and external to UHS. You will utilise your clinical skills and research expertise through set-up and delivery and help to inform and support management of the team.

The role will involve screening, recruiting and follow-up of potential and enrolled participants at Southampton. You will work alongside our current team of Research Sisters/AHPs/Midwives who are committed to driving forward the research strategy here at UHS.  

Enthusiasm, self-motivation, flexibility and drive will be required to ensure the success of this post and the PICNIC study. You will need excellent time management skills and must be able to troubleshoot and problem solve to ensure the smooth set-up and running of PICNIC supporting the Project Manager.  Excellent communication skills are required to provide guidance and support to the 3 UK R&D departments, clinicians and the research delivery teams, liaising with research and clinical colleagues across departments.  The ability to communicate with staff and colleagues at all levels and disciplines in an engaging manner is essential.  Good IT skills will be required. 
   

We currently have a vacancy for a 0.5WTE (18.75hrs/week) Band 6 research role, to be worked over a minimum of 3 days. This is an exciting opportunity to take up a new position supporting the set-up and management of a locally designed, multicentre study for heart attack patients. The PICNIC Study was designed and is led by Chief Investigator Professor Nick Curzen, Professor of Interventional Cardiology. PICNIC will recruit patients presenting with a heart attack – ST-Elevation Myocardial Infarction (STEMI). Through the development of an artificial intelligence program, PICNIC aims to risk stratify future patients presenting with STEMI and offer a tailored, more personalised treatment plan to reduce the risk of potential future clinical events such as further heart attacks, strokes and heart failure.

The role will initially focus on supporting trial set-up in collaboration with the Chief Investigator and Project Manager and will include:

•    Support trial set-up in collaboration with the Chief Investigator, Project Manager and other relevant personnel.  This will include contributing to patient-facing and study documents.
•    Working with the Project Manager and Sponsor to ensure regulatory requirements are fulfilled and that all approvals and authorisations are in place for UK sites.
•    Taking responsibility for applications as appropriate and assisting/advising participating investigators with local study requirements.
•    Establishing links with key members of staff at the UK centres and ensuring essential documentation is in place.
•    Monitoring trial conduct as appropriate to ensure protocol compliance, good patient management and ensuring Good Clinical Practice guidelines are adhered to.
•    Acting as the main point of contact for PICNIC.
•    Explaining promoting the trial (including newsletter production, website updates) to ensure wide participation and good accrual of and participants.  
•    Writing and submitting trial progress reports as and when required, including reports for trial funders and the Research Ethics Committee
•    Screening, recruiting and follow-up of PICNIC participants at UHS