Paediatric Research Nurse

NHS; London; On-site; GBP 37,000 - 45,000; Full time

Job summary

An exciting opportunity at Lewisham and Greenwich NHS Trust for a Research Nurse within Children's Services. This role involves coordinating research studies, working alongside paediatric specialists to manage recruitment, and ensuring excellent patient care and adherence to clinical trial protocols. Join a supportive team dedicated to advancing clinical research for children's health.

Qualifications

• Educated to degree level in a health-related discipline.
• Prior experience in paediatrics and clinical research is essential.
• Experience of effective multi-disciplinary team working.

Responsibilities

• Coordinate research studies and manage patient recruitment.
• Ensure compliance with Good Clinical Practice guidelines.
• Supervise data collection and entry for clinical trials.

Skills

Team collaboration

Clinical research

Patient care

Education

Degree in health or social sciences

GCP trained

Clinical Research Qualification

Job description

Lewisham and Greenwich NHS Trust is a research-active organisation with a proven track-record in clinical research. We are committed to developing our research portfolio and to enable this we are strengthening our research infrastructure.

This role involves working cross-site at University Hospital Lewisham and Queen Elizabeth Hospital, Woolwich and the successful candidate would be managed jointly between the Paediatric and R& D teams.

We are currently looking for a nurse with an interest in Children's research to be part of our team in Children's Services to coordinate the multiple research studies that we have enrolled in alongside the Consultant with an interest in research and the research department.

You will be a part of a friendly, passionate and supportive Research and Development team working together to support the delivery of NIHR portfolio studies and Commercial research studies. It is important that the applicant is self-motivated and has a keen interest in clinical research. Prior experience of working in paediatrics is essential for this role but having research experience is desirable.

Previous applicants need not apply.

Main duties of the job

The role involves working closely alongside the multi-disciplinary team and the research participants and their families. Central to the role is recruitment- undertaking all aspects of a clinical research trial including screening and assessing patient eligibility for the trial, obtaining informed consent, carrying out study procedures, entering study data, undertaking study follow ups in accordance with study protocol. The successful applicant will be responsible for ensuring that any research undertaken within the department safeguards the well-being of the patients and is conducted within ICH Good Clinical Practice Guidelines for Research.

About us

Our people are our greatest asset. When we feel supported and happy at work, this positivity reaches those very people we are here for, the patients. Engaged employees perform at their best and our Equality, Diversity & Inclusion (EDI) initiatives contribute to cultivate a culture of engagement. We have four staff networks, a corporate EDI Team and a suite of programmes and events which aim to insert the 5 aspirations:

• Improving representation at senior levels of staff with disabilities, from black, Asian, and ethnic minorities background, identify as LGBTQ+ and women, through improved recruitment and leadership development
• Widening access (anchor institution) and employability
• Improving the experience of staff with disability
• Improving the EDI literacy and confidence of trust staff through training and development
• Making equalities mainstream

Job responsibilities

The post holder will: be responsible for the day to day management of a portfolio of studies at the Trust, work with colleagues to promote and facilitate research activity within the trust support the R&D Delivery Manager in achieving the team objectives to develop and extend the range of research undertaken support and supervise the trust Clinical Trial Co-ordinators and work with the network delivery staff Work with colleagues to implement the recruitment plans

Key Result Area 1 Service Management:

Support the R&D Delivery Manager in delivery of recruitment into clinical trials, including assisting investigators to determine recruitment targets during study set-up and feasibility assessment

Evaluate clinical trial protocols in close liaison with Principal Investigators and research managers, identifying implications for service support, changes in treatment and completing feasibility assessments

Develop and maintain relationships with the trust staff in Service Support departments ( e.g. Pharmacy, Radiology and Laboratory services)

Ensure a study site master file is set up and properly maintained for each trial

Identify patients suitable for entry into trials by attending clinics, screening notes, attending multi-disciplinary team meetings and using clinical databases

Ensure patients are fully informed prior to entry in any clinical trial and provide them with reassurance and support

Assist in consenting, randomising and allocating of treatment of patients

Collect biological samples e.g. blood required as part of the protocol and ensure safe and appropriate storage and shipment of specimens

Co-ordinate the accurate completion of Case Report Forms (CRFs) in conjunction with the Clinical Trial Co-ordinators

Assisting investigators in the timely completion of clinical research files and resolution of data queries

Ensure the study recruitment figures are reported weekly onto the EDGE database in accordance with local and national requirements

To supervise the patient follow-up process and provide supportive care

Support the trust in meeting national R&D standards including the Research Governance Framework, Good Clinical Practice (GCP), Information Governance, Data Protection Act etc;

Prioritise patient safety and the well-being of clinical trial participants at all times

Represent Research & Development and the trust at meetings with external organisations including sponsors and monitors as required

Develop plans and monitor trial recruitment and develop suitable interventions for under-recruiting studies;

Ensure that patient data is protected according to the Data Protection Act 1998

Support the R&D Delivery Manager in investigating any concerns around the conduct of clinical trials and escalating within the Senior Management team, Clinical Director and sponsor as appropriate

Person Specification

Experience

• Experience of effective multidisciplinary team working
• Experience of working in a research role
• Experience of setting up research projects and facilitating recruitment to them
• Experience of patient care and follow-up within research studies
• Experience of managing staff

Qualifications and Training

• Educated to degree level in a health related or social sciences discipline or equivalent experience
• GCP trained
• Clinical Research Qualification

Disclosure and Barring Service Check

This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.

£37,338 to £44,962 a yearper annum pro rata plus HCAS