Job summary
An exciting opportunity has arisen for an enthusiastic, motivated and experienced Research Nurse / Coordinator, with excellent planning and organisational skills to join our research team at Northwick Park Hospital
The LNWH is a research active Trust. The research teams and R&D are committed to improving healthcare services by promoting and supporting a wide range of high quality research.
The role will involve setting up and coordinating clinical studies, delivering on key objectives and developing research capacity within the Research and development. You will recruit patients into studies and be responsible for all aspects of the studies or enrolment and data collection. You will work collaboratively with the clinical studies team and the wider multi-disciplinary team (MDT) in the management of clinical trials.
The post holder will be expected to be proactive in educating clinical staff in the specifics of running clinical trials. You should demonstrate the ability to manage own work load and to work as part of a team.
Previous experience working within a clinical research environment will be desirable. This post offers excellent opportunities in gaining managerial experience and the opportunity to maintain your clinical skills.
Main duties of the job
The post holder will be responsible for assessing and managing the care pathways for patients and carers participating in clinical studies. This will involve the recruitment, education and monitoring of patients in studies and the collection and documentation of accurate data. You will work collaboratively with different clinical studies team and the wider multi-disciplinary team (MDT) in the management of your own caseload of patients in clinical research studies.
The post holder will participate in the process of supporting the consent process, including the explanation of standard and research treatment, risks, benefits and side effects. She/he will be responsible for randomisation, completion of case report forms (CRFs) and the maintenance of accurate records according to ICH-GCP (Good Clinical Practice). The post holder will also have responsibility for the organisation of investigations, tracking follow-up of patients, entering data and making regular submissions of data to clinical trials centres and the R&D Department. The post holder will be expected to be proactive in educating clinical staff in the specifics of running clinical trials. Willingness to work flexibly is an essential aspect of this post.
Although the post holder will be based at Central Middlesex hospital they will be expected to work flexibly across the Trust.
About us
London North West University Healthcare NHS Trust (LNWH) cares for the people of Brent, Ealing, Harrow and beyond.
Our team of more than 8,200 clinical and support staff serve a diverse population of almost one million people.
We run major acute services at:
o Northwick Park Hospital: home to one of the busiest emergency departments (A&E) in the country. The hospital provides a full range of services including the country's top-rated hyper-acute stroke unit and one of only three hyper-acute rehabilitation units in the UK
o St Mark's Hospital: an internationally renowned specialist centre for bowel disease
o Ealing Hospital: a busy district general hospital providing a range of clinical services, as well as 24/7 emergency department and urgent care centre, and specialist care at Meadow House Hospice
o Central Middlesex Hospital: our planned care site, hosting a range of surgical and outpatient services and collocated with an urgent care centre.
We are a university teaching NHS trust, in recognition of the important role we play in training clinicians of the future and bringing the benefits of research to the public.
Job description
Job responsibilities
Please review job description for further details.
Duties will also include;
Identification of patients who are suitable for entry into clinical trials and plan the care and support of patients according to clinical trial protocols, and to monitor responses throughout the trial
Communicate with other research nurse and co-ordinators within the Trust and develop good working relations to help support them where necessary and encourage a good working relationship with the medical doctors and nurses involved in patient care and facilitate a team approach to patient recruitment/enrolment to trials and safe practice.
Work at all times according to regulations as described in ICH, Good Clinical Practice (GCP), and to the most current guidance relating to research governance and research ethics in each Trust and liaise with Clinical Trial Offices and external investigators and designated staff within supporting departments when necessary to set up and coordinate research studies.
Support the research strategy of the Trust.
To view the main responsibility, please see the attached the Job Description and Person Specification.
Person Specification
Education and Qualification
Essential
1. oRegistered Nurse or possession of a relevant degree
2. oCurrent good clinical research practice course (ICH-GCP)
Knowledge and Experience
Essential
3. able to demonstrate they have the ability to work in a clinical environment
4. oExperience of managing and Coordinating patient care
Desirable
5. oPrevious experience in working in clinical research
Skills and abilities
Essential
6. oAbility to acquire in-depth knowledge of trial protocols and to communicate this to professionals and lay persons
7. able to work unsupervised as part of team
Desirable
8. be flexible and adapt to the service need