Clinical Research Nurse

Job description

Job summary

Through the NIHR Barts BRC and Barts BioResource (BBR), we develop digital health technologies, cardiovascular devices, precision medicine programmes and large-scale clinical research studies to improve patient care.

We are seeking an enthusiastic Band 6 Research Nurse to join our team. The role offers involvement in a portfolio of studies including digital health, AI, wearable technologies, innovative interventions, medical devices and biobanking.

You will support delivery of the NIHR Barts BRC Precision Digital Health, Cardiovascular Devices and Trials Theme and the expansion of BBR, a programme collecting linked health data and biological samples to support future research.

Working within a multidisciplinary team, you will coordinate research studies from set-up to close-out, support participant recruitment and consent, collect research data and biosamples, manage study delivery and governance, and contribute to integrating research into routine NHS care.

Essential

o Current NMC registration.o Experience in cardiology, cardiac care, critical care or a related specialty.o Excellent organisational, communication and IT skills.o Ability to manage multiple projects independently.o Enthusiasm for patient-centred research.

Desirable

o Clinical research experience.o Research governance knowledge.o Experience with medical devices, digital health studies or biosamples.

Maria Vourvou: 0203 765 8704 | [email protected]

Main duties of the job

oCoordinating clinical research studies from set-up through to close-out.oSupporting participant identification, recruitment, informed consent and follow-up.oAssisting with the delivery of the Barts BioResource, including participant enrolment, biosample collection, processing and management.oCollection, maintenance and accurate entry of research data across a variety of clinical and digital research platforms.oSupporting studies involving digital health technologies, wearable devices, AI-enabled tools, cardiovascular devices, precision medicine initiatives and innovative clinical trials.oEducating patients, carers and clinical colleagues about research studies and opportunities for participation.oActing as a patient advocate, ensuring participants receive clear and appropriate information to make informed decisions regarding research involvement.oEnsuring adherence to Good Clinical Practice (GCP), study protocols, Trust policies, information governance requirements and regulatory standards.

The successful candidate will contribute to nationally leading programmes in precision digital health, cardiovascular innovation, advanced clinical trials and large-scale translational research, helping to deliver research that improves outcomes for the diverse populations served by Barts Health NHS Trust.

About us

Barts Health is one of the largest NHS trusts in the country, and one of Britain's leading healthcare providers.

Our vision is to be a high-performing group of NHS hospitals, renowned for excellence and innovation, and providing safe and compassionate care to our patients in east London and beyond. That means being a provider of excellent patient safety, known for delivering consistently high standards of harm-free care and always caring for patients in the right place at the right time. It also means being an outstanding place to work, in which our WeCare values and behaviours are visible to all and guide us in how we work together.

We strive to live by our WeCare values and are committed to promoting inclusion, where every staff member has a sense of belonging. We value our differences and fully advocate, cultivate and support an inclusive working environment.

Job description

Job responsibilities

The full job description provides an overview of the key tasks and responsibilities of the role, and the person specification outlines the qualifications, skills, experience, and knowledge required. For both documents, please view the attachment/s below.

Job description
Job responsibilities

The full job description provides an overview of the key tasks and responsibilities of the role, and the person specification outlines the qualifications, skills, experience, and knowledge required. For both documents, please view the attachment/s below.

Person Specification

Qualifications

Essential

• Registered Nurse with current NMC registration
• Intravenous accreditation
• Teaching / Mentorship course or equivalent
• Possession of / or can demonstrate equivalence to an undergraduate degree in Nursing, Science or Health related discipline

Desirable

• Research qualification
• Good Clinical Practice certification
• ALS/ILS or equivalent

Experience

Essential

• Experience in Cardiology or Cardiac/Critical care nursing
• Experience in clinical, organisational and team management
• Experience of working as part of a multidisciplinary team
• Experience of explaining complex concepts to patients in a clear and simplified manner
• Experience of formal/ informal teaching of patients and staff
• Experience of managing physically and emotionally challenging patient cohorts and environments

Desirable

• Experience in Research Nursing in Clinical investigations or trials
• Project management experience
• Experience of clinical trial data entry on multiple platforms

Knowledge

Essential

• Broad knowledge and experience of post registration nursing practice within an acute hospital environment
• Evidence of continuous personal

Desirable

• Knowledge and experience of Research Governance, EU Clinical Trials Directive, Directive 93/42/EEC on medical devices (EU MDD) and Good Clinical Practice.
• Basic statistical knowledge
• Knowledge of Trials Research Management Software e.g. EDGE

Skills

Essential

• Proactive and self- motivated with ability to lead, motivate and empower others.
• Well-developed interpersonal and Communication skills including: interpersonal, liaison and negotiating skills.
• Ability to confront challenging issues taking a problem-solving approach.
• Ability to produce clear, accurate written and verbal reports.
• Ability to prioritise, meet tight deadlines and work independently on a number of projects
• Ability to work in a multi- professional arena.
• Attention to detail and meticulous, accurate documentation
• Computer literacy

Desirable

• Ability to lead and manage meetings effectively.
• Has some budgetary and resources management skills
• Phlebotomy and cannulation skills

Other

Essential

• Willingness to work flexible hours on occasion
• Displays enthusiastic and proactive approach to work
• Enthusiasm for and desire to embed research in clinical practice
• Able to articulate reason

Person Specification
Qualifications

Essential

• Registered Nurse with current NMC registration
• Intravenous accreditation
• Teaching / Mentorship course or equivalent
• Possession of / or can demonstrate equivalence to an undergraduate degree in Nursing, Science or Health related discipline

Desirable

• Research qualification
• Good Clinical Practice certification
• ALS/ILS or equivalent

Experience

Essential

• Experience in Cardiology or Cardiac/Critical care nursing
• Experience in clinical, organisational and team management
• Experience of working as part of a multidisciplinary team
• Experience of explaining complex concepts to patients in a clear and simplified manner
• Experience of formal/ informal teaching of patients and staff
• Experience of managing physically and emotionally challenging patient cohorts and environments

Desirable

• Experience in Research Nursing in Clinical investigations or trials
• Project management experience
• Experience of clinical trial data entry on multiple platforms

Knowledge

Essential

• Broad knowledge and experience of post registration nursing practice within an acute hospital environment
• Evidence of continuous personal

Desirable

• Knowledge and experience of Research Governance, EU Clinical Trials Directive, Directive 93/42/EEC on medical devices (EU MDD) and Good Clinical Practice.
• Basic statistical knowledge
• Knowledge of Trials Research Management Software e.g. EDGE

Skills

Essential

• Proactive and self- motivated with ability to lead, motivate and empower others.
• Well-developed interpersonal and Communication skills including: interpersonal, liaison and negotiating skills.
• Ability to confront challenging issues taking a problem-solving approach.
• Ability to produce clear, accurate written and verbal reports.
• Ability to prioritise, meet tight deadlines and work independently on a number of projects
• Ability to work in a multi- professional arena.
• Attention to detail and meticulous, accurate documentation
• Computer literacy

Desirable

• Ability to lead and manage meetings effectively.
• Has some budgetary and resources management skills
• Phlebotomy and cannulation skills

Other

Essential

• Willingness to work flexible hours on occasion
• Displays enthusiastic and proactive approach to work
• Enthusiasm for and desire to embed research in clinical practice
• Able to articulate reason

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 .

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. .
UK Registration

Applicants must have current UK professional registration. For further information please see

Additional information
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 .

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. .
UK Registration

Applicants must have current UK professional registration. For further information please see

Employer details

Employer name

Barts Health NHS Trust
Address

St Bartholomew Hospital

London

EC1A 7BE

United Kingdom

Employer's website