Clinical Research Nurse - Critical Care

Guy's and St Thomas' NHS Foundation Trust

This job is now closed

Job summary

Are you looking for a new challenge to progress you career within Research nursing? Do you think you could contribute to a busy and dynamic clinical research team? We are looking for a dynamic and highly motivated nurse to join our friendly Critical Care research team. You should have excellent communication and interpersonal skills and have the ability and initiative to work independently. You should be able to manage your workload flexibly across a range of projects and deadlines in a fast-pace working environment.

Main duties of the job

You will be an essential member of the Critical Care research team, leading a growing portfolio of observational research and clinical trials of investigational medicines & devices within this specialty. The role will include supporting the delivery of commercial and non-commercial studies. You will work closely with a dynamic multi-disciplinary research team to deliver our portfolio of studies. You will be required to liaise with trial site coordinators for site initiation visits, site visits and site closures as appropriate. You will be required to attend research meetings on a regular basis.

About us

There are excellent opportunities for further education and research development as part of these roles, with access to CPD funding and revalidation support. Opportunities for developing new research and clinical skills are available and actively encouraged.

Date posted

11 September 2023

Pay scheme

Agenda for change

Band

Band 6

Salary

£42,471 to £50,364 a year p.a. inclusive of HCA (pro rata)

Contract

Fixed term

Duration

12 months

Working pattern

Full-time

Reference number

196-BRC2011

Job locations

St Thomas' Hospital

London

SE1 7EH

Job description

Job responsibilities

CLINICAL:

Work with the team to manage and coordinate and support existing and new portfolio of clinical research whilst working as part of a multidisciplinary team. Maintaining effective communication with patients, carers and professionals to ensure service delivery. Assist in selecting, screening and organising the patients and/or volunteers suitable for entry into clinical trials/studies when applicable.
Act as a resource and support to patients and their relatives, explaining practical aspects of the trial or study, assisting and supporting local nursing teams.
Coordinate the collection of all biological samples required as part of the clinical trial/study and ensure safe and appropriate storage of specimens, in conjunction with Sponsors.
Ensure the safe administration of trial drugs, have knowledge of the legal requirements of a clinical trial sponsor regarding pharmacovigilance and of the Trust pharmacovigilance policy. Report any adverse events and reactions in accordance with this policy and the trial protocol.
At all times to ensure clear, accurate records are maintained by the team.
Implement and adhere to the principles of Good Clinical Practice (GCP) and ensure that all trials are conducted according to the Medicines for Human Use (Clinical Trial) Regulations 2004 and Amended Regulations 2006 where appropriate.
To oversee the routine maintenance and servicing of clinical equipment as appropriate

MANAGEMENT:

To represent Guys and St Thomas NHS Foundation Trust as a research nurse in external situations, for example national and international conferences, committees etc. as appropriate.
To report any adverse incident/near misses in relation to that activity to peers and external stakeholders as required
To facilitate and maintain effective communication within the clinical and research team.
To responsibly support the control of equipment, resources and stock through the adherence of research policies and clinical trials budgets.

EDUCATION:

Ensure mandatory clinical trials training is undertaken and updated as required.
To be responsible for developing and sustaining own knowledge, clinical skills and professional awareness.

PROFESSIONAL:

You will be accountable for your own professional actions, acting within clearly defined policies/procedures and codes of conduct including the NMC code and Trust policy.
To act in accordance with local policies and procedures laid down by Guys and St Thomas NHS Foundation Trust and ensure that all mandatory training for nursing staff within the Trust is attended.
To work within the NMC Scope of Professional Practice and Code of Conduct.
To undertake Performance Development Review annually to identify organisational and professional objectives and developmental needs.
To keep up to date with departmental, Trust, NHS, academic and EU developments for the management of clinical research ensuring timely, effective implementation of changes.
To attend courses as deemed relevant, including mandatory training, and to attend meetings and conferences as appropriate

Job description

Job responsibilities

CLINICAL:

Work with the team to manage and coordinate and support existing and new portfolio of clinical research whilst working as part of a multidisciplinary team. Maintaining effective communication with patients, carers and professionals to ensure service delivery. Assist in selecting, screening and organising the patients and/or volunteers suitable for entry into clinical trials/studies when applicable.
Act as a resource and support to patients and their relatives, explaining practical aspects of the trial or study, assisting and supporting local nursing teams.
Coordinate the collection of all biological samples required as part of the clinical trial/study and ensure safe and appropriate storage of specimens, in conjunction with Sponsors.
Ensure the safe administration of trial drugs, have knowledge of the legal requirements of a clinical trial sponsor regarding pharmacovigilance and of the Trust pharmacovigilance policy. Report any adverse events and reactions in accordance with this policy and the trial protocol.
At all times to ensure clear, accurate records are maintained by the team.
Implement and adhere to the principles of Good Clinical Practice (GCP) and ensure that all trials are conducted according to the Medicines for Human Use (Clinical Trial) Regulations 2004 and Amended Regulations 2006 where appropriate.
To oversee the routine maintenance and servicing of clinical equipment as appropriate

MANAGEMENT:

To represent Guys and St Thomas NHS Foundation Trust as a research nurse in external situations, for example national and international conferences, committees etc. as appropriate.
To report any adverse incident/near misses in relation to that activity to peers and external stakeholders as required
To facilitate and maintain effective communication within the clinical and research team.
To responsibly support the control of equipment, resources and stock through the adherence of research policies and clinical trials budgets.

EDUCATION:

Ensure mandatory clinical trials training is undertaken and updated as required.
To be responsible for developing and sustaining own knowledge, clinical skills and professional awareness.

PROFESSIONAL:

You will be accountable for your own professional actions, acting within clearly defined policies/procedures and codes of conduct including the NMC code and Trust policy.
To act in accordance with local policies and procedures laid down by Guys and St Thomas NHS Foundation Trust and ensure that all mandatory training for nursing staff within the Trust is attended.
To work within the NMC Scope of Professional Practice and Code of Conduct.
To undertake Performance Development Review annually to identify organisational and professional objectives and developmental needs.
To keep up to date with departmental, Trust, NHS, academic and EU developments for the management of clinical research ensuring timely, effective implementation of changes.
To attend courses as deemed relevant, including mandatory training, and to attend meetings and conferences as appropriate

Person Specification

Knowledge/Qualifications

Essential

Educated to degree level or above

Desirable

A Clinical Research qualification

Previous experience

Essential

Extensive experience of working within an acute adult ward environment as a qualified nurse with previous ICU NHS experience.
Experience with a variety of computer programmes, including Access, Excel, Micrsoft office, Outlook and databases

Desirable

Experience in Clinical Research
Familiar with Good Clinical Practice & Certification

Skills

Essential

Competency in medication administration including IV drugs
Organisation and management skills.

Desirable

Knowledge of research methodologies

Other

Essential

Enthusiastic, professional and accountable for own actions.

Person Specification

Knowledge/Qualifications

Essential

Educated to degree level or above

Desirable

A Clinical Research qualification

Previous experience

Essential

Extensive experience of working within an acute adult ward environment as a qualified nurse with previous ICU NHS experience.
Experience with a variety of computer programmes, including Access, Excel, Micrsoft office, Outlook and databases

Desirable

Experience in Clinical Research
Familiar with Good Clinical Practice & Certification

Skills

Essential

Competency in medication administration including IV drugs
Organisation and management skills.

Desirable

Knowledge of research methodologies

Other

Essential

Enthusiastic, professional and accountable for own actions.

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.

Certificate of Sponsorship

Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).

From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).