The primary role of the Clinical Research Assistant is to support the portfolio of clinical research studies based at the Liverpool Heart and Chest Hospital.
You will be responsible for facilitating the research pathways of patients participating in research studies.
You will be directly involved in recruitment, education and the monitoring of research patients and the collection and documentation of accurate data.
You will provide support for a specific research study but may be required to support the wider research portfolio when necessary. There will be a requirement for travelling across the Merseyside and Cheshire region to support the recruitment to this research study and transport will be provided. The base is considered as Liverpool Heart and Chest Hospital.
You will work collaboratively with the multi-disciplinary teams across the Trust and community.
Operate independently without supervision within the defines of your pay Band
Manage own time and workload with an overview from senior staff
Plan, deliver and evaluate patient-centred care in relation to the study protocol
Manage patient clinics within a studies requirement
Inform study patients GPs of their participation in a clinical trial,
Collect, collate, and report information, maintaining accurate patients records in line with Trust policy including Information Governance, Study Protocols and ICH_GCP.
Participate in maintaining a safe, comfortable therapeutic environment for all patients and carers.
Work collaboratively with other professionals and agencies to ensure needs are met in relation to care input and support for ongoing care needs.
Establish and maintain effective communication with patients and carers/family members consistent with their level of understanding and their culture.
Respect confidential information obtained in the course of professional practice and uphold the principles of Caldicott and the Data Protection Act.
Complete documentation via the electronic patient record system in line with Trust Policy, and Information Governance and ICH-GCP guidelines.
Undertake venepuncture and sample collection following training and assessment.
Stock taking and ordering consumables.
Sample kit coordination and dispatch.
Consent to research studies following training and delegation of task.
As the largest single site specialist heart and chest hospital in the UK, we, at Liverpool Heart and Chest Hospital, have a clear vision 'to be the best cardiothoracic integrated healthcare organisation'.
We provide specialist services in cardiothoracic surgery, cardiology, respiratory medicine both in the hospital and out in the community.
We serve a catchment area of 2.8 million people, spanning Merseyside, Cheshire, North Wales and the Isle of Man, and increasingly we receive referrals from outside these areas for highly specialised services such as aortics.
Our reputation for strong performance is important in delivering the best care for our patients and high quality clinical services. This is underpinned by a culture of research and innovation, delivered in modern estate and our encouragement of flexible working in a variety of forms.
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CLINICAL
Operate independently without supervision within the defines of your pay Band
Manage own time and workload with an overview from senior staff
Plan, deliver and evaluate patient-centred care in relation to the study protocol
Manage patient clinics within a studies requirement
Inform study patients GPs of their participation in a clinical trial, liaising with the GP as required
Collect, collate, and report information, maintaining accurate patients records in line with Trust policy including Information Governance, Study Protocols and ICH_GCP.
Participate in maintaining a safe, comfortable therapeutic environment for all patients and carers.
Work collaboratively with other professionals and agencies to ensure needs are met in relation to care input and support for ongoing care needs.
Establish and maintain effective communication with patients and carers/family members consistent with their level of understanding and their culture.
Assess the potential risks involved within the scope of work activities, identifying how best to manage the risks.
Respect confidential information obtained in the course of professional practice and uphold the principles of Caldicott and the Data Protection Act.
Complete documentation via the electronic patient record system in line with Trust Policy, and Information Governance and ICH-GCP guidelines.
Undertake venepuncture and sample collection following training and assessment.
Stock taking and ordering consumables.
Sample kit coordination and dispatch.
Consent to research studies following training and delegation of task.
STUDY REQUIREMENTS
Assembling, completing, and maintaining the required regulatory documentation in a clear and organised way
Ensure that the study is conducted adhering to the International Conference for Harmonisation (ICH) and Good Clinical Practise (GCP) guidelines, UK Clinical Trials Regulations and in accordance with its protocol
Attend Investigator meetings and set up meetings.
Liaise with the Principal Investigator to ensure study delivery
Identify and screen for potential research participants
Be able to advise and support patients and their families when considering participation in a study
Ensure availability of clear and easy to follow study guidelines, so that staff workload is kept to a minimum
Obtain informed consent from study participants in line with GCP Guidelines and study protocol.
To prioritise research activity as necessary thus ensuring recruitment targets are met.
To ensure that all data is collected and managed effectively and accurately.