Job summary
The
Haematology Clinical Trials Team is part of the National Institute for Health
Research (NIHR) Clinical Research Network: Yorkshire & the Humber. Leeds is also one of the leading sites in
the UK looking into the research, diagnostics and treatment development of
haematological disorders.
The
Haematology Clinical Trials Department offers a busy and dynamic environment,
supporting the delivery of clinical research across a wide range of malignant
and non-malignant diseases. An opportunity has arisen for an enthusiastic,
motivated Nurse to join a team of clinicians, nurses and supporting staff to
provide patients with the opportunity to participate in clinical studies.
Main duties of the job
The
post will be based at St Jamess Institute of Oncology, Level 3 Bexley Wing,
St James University Hospital Leeds. The aim of the post is to support the
department deliver a portfolio of clinical trials to a high standard, working
with colleagues within the Clinical Trials department, Trust and external
organisations.
.
The
successful candidate will be responsible for the the coordination and
management of patients being considered for, and participating in clinical
trials. The role will involve patient
recruitment, the delivery of SACT and non SACT investigational treatments,
and the continued assessment of patients throughout trials. The department manages a large and complex
portfolio of clinical studies,
actively delivering early phase 1 through to high recruiting phase 3
trials.
About us
For
the right candidate this post offers the opportunity to acquire new knowledge
and experience in the world of Research Nursing, The work is varied,
interesting, and at times, challenging. You will be supported by a large
and experienced team of Haematology
Research Nurses, and you will derive satisfaction from a contribution that
makes real differences to patients lives as well as the development of new
treatments
The
post sits within the well-established Haematology Research Nurse Team. The team maintains a close working
relationship with the Leeds Clinical Research Facility (LCRF), and the post
holder will be involved in supporting a cross section of early phase clinical
trials conducted in the LCRF.
Leeds
Teaching Hospitals is committed to our process of redeploying 'at risk'
members of our existing workforce to new roles. As such, all our job adverts
are subject to this policy and we reserve the right to close, delay or remove
adverts while this process is completed. If you do experience a delay in the
shortlisting stage of the recruitment cycle, please bear with us while this
process is completed, and contact the named contact if you have any
questions.
Job description
Job responsibilities
The
post holder will contribute actively to the conduct, coordination and
delivery of the Haematology Trials Research Portfolio, under the leadership
of the Senior Research Nurse/Midwife. Working effectively with the immediate
and broader multidisciplinary team (MDT), being responsible for ensuring that
high standards of clinical care planning, delivery, safety and patient
satisfaction is to a very high standard, compliant with Trust policy, study
protocol requirements, local and national guidance and legislation.
The
post holder will support the Senior Research Nurse/Midwife, Principle
Investigators and associated multidisciplinary colleagues in the planning,
scheduling, conduct, recruitment, patient care, support and data collection
required for all studies within the department. They will be responsible for
developing their own clinical practice, maintaining competencies (related to
the research portfolio) and where appropriate taking delegated responsibility
for the clinical elements of studies in line with Trust policies and study
protocols.
Working
effectively and proactively with agreed external agencies and collaborative
partners, the individual will adhere to agreed study pathways and processes
to derive accurate and robust data capture, and ensure pharmacovigilance is
maintained.
The
post holder will be involved in ensuring that research undertaken within the
department safeguards the wellbeing of patients and is conducted within the
confines of ICH Good Clinical Practice Guidelines for Research, EU directive,
UK Governance Framework and other relevant UK legislation pertaining to the
conduct and delivery of research.
The
post holder will act as a role model developing the research team and
ensuring effective management of the department in the absence of the Senior
Research Nurse/Midwife. During exceptional times of need, you will contribute
to clinical service, as agreed with the Matron for the CSU and in line with
the Trusts escalation policy.
We
are looking to recruit a proactive and self-motivated, individual with a keen
interest in research to work within the Haematology Clinical Trials team. The
post-holder will work closely with senior colleagues and members of the MDT
to deliver high quality clinical care to patients during their participation
in both interventional and observational studies. The post will cover both
the inpatient and outpatient settings with the caseload varying in size and
complexity according to the trial portfolio.
The
post holder will be required to work alongside industry partners, the
National Institute for Health Research (NIHR) Clinical Research Network (CRN)
Yorkshire and Humber (Y&H) and colleagues in neighbouring establishments,
attending regional and national meetings as required.
Job description
Job responsibilities
The
post holder will contribute actively to the conduct, coordination and
delivery of the Haematology Trials Research Portfolio, under the leadership
of the Senior Research Nurse/Midwife. Working effectively with the immediate
and broader multidisciplinary team (MDT), being responsible for ensuring that
high standards of clinical care planning, delivery, safety and patient
satisfaction is to a very high standard, compliant with Trust policy, study
protocol requirements, local and national guidance and legislation.
The
post holder will support the Senior Research Nurse/Midwife, Principle
Investigators and associated multidisciplinary colleagues in the planning,
scheduling, conduct, recruitment, patient care, support and data collection
required for all studies within the department. They will be responsible for
developing their own clinical practice, maintaining competencies (related to
the research portfolio) and where appropriate taking delegated responsibility
for the clinical elements of studies in line with Trust policies and study
protocols.
Working
effectively and proactively with agreed external agencies and collaborative
partners, the individual will adhere to agreed study pathways and processes
to derive accurate and robust data capture, and ensure pharmacovigilance is
maintained.
The
post holder will be involved in ensuring that research undertaken within the
department safeguards the wellbeing of patients and is conducted within the
confines of ICH Good Clinical Practice Guidelines for Research, EU directive,
UK Governance Framework and other relevant UK legislation pertaining to the
conduct and delivery of research.
The
post holder will act as a role model developing the research team and
ensuring effective management of the department in the absence of the Senior
Research Nurse/Midwife. During exceptional times of need, you will contribute
to clinical service, as agreed with the Matron for the CSU and in line with
the Trusts escalation policy.
We
are looking to recruit a proactive and self-motivated, individual with a keen
interest in research to work within the Haematology Clinical Trials team. The
post-holder will work closely with senior colleagues and members of the MDT
to deliver high quality clinical care to patients during their participation
in both interventional and observational studies. The post will cover both
the inpatient and outpatient settings with the caseload varying in size and
complexity according to the trial portfolio.
The
post holder will be required to work alongside industry partners, the
National Institute for Health Research (NIHR) Clinical Research Network (CRN)
Yorkshire and Humber (Y&H) and colleagues in neighbouring establishments,
attending regional and national meetings as required.
Person Specification
Qualifications
Essential
- Registered Adult Nurse
- Post registration qualification in speciality
Desirable
- Recognised teaching/ assessing qualification
- Research qualification (e.g. certificate/ MSc in clinical research)
Experience
Essential
- Significant post registration experience
- Experience of computer databases and administration
Desirable
- Research experience
- Haematology experience
Skills & Behaviours
Essential
- Willing to undergo training as necessary
- Knowledge of clinical research specific issues
- Autonomy Independence
- Capable of lateral thinking
- IT skills
- Excellent Time management Skills
- Excellent communication and interpersonal skills
- SACT competent
Desirable
- Awareness and understanding of the principles of ICH GCP
practical skills or Additional Requirements
Essential
- Able to fulfil Occupational health requirements for post
Person Specification
Qualifications
Essential
- Registered Adult Nurse
- Post registration qualification in speciality
Desirable
- Recognised teaching/ assessing qualification
- Research qualification (e.g. certificate/ MSc in clinical research)
Experience
Essential
- Significant post registration experience
- Experience of computer databases and administration
Desirable
- Research experience
- Haematology experience
Skills & Behaviours
Essential
- Willing to undergo training as necessary
- Knowledge of clinical research specific issues
- Autonomy Independence
- Capable of lateral thinking
- IT skills
- Excellent Time management Skills
- Excellent communication and interpersonal skills
- SACT competent
Desirable
- Awareness and understanding of the principles of ICH GCP
practical skills or Additional Requirements
Essential
- Able to fulfil Occupational health requirements for post
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.
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).
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.
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).