Job summary
  
 
 
 A
 fantastic opportunity has arisen for an enthusiastic, experienced and
 motivated Senior Research Nurse to join the Haematology Clinical Trials team
 on a 12-month fixed-term contract or secondment. The successful candidate
 will lead and co-ordinate a large portfolio of clinical trials involving
 Early Phase/First in Human, Late Phase, Experimental Medicine and Advanced
 Therapy Investigational Medicinal Products (ATIMPs).
 
 This
 complex and interesting portfolio is rapidly evolving and expanding to
 include a multitude of different investigational products across multiple
 malignant and non-malignant haematological disease specialties, testing new
 treatments, new techniques and new devices to potentially benefit
 patients. 
 
 We
 are looking for a dynamic individual who will provide leadership and
 management with specialist expertise and professional knowledge and holds
 excellent communication and interpersonal skills. 
 
 
 
 Expected Shortlisting
 Date
 
 
 03/11/2025
 
 
 
 
 Planned Interview
 Date
 
 
 10/11/2025
  Main duties of the job
  
 
 
 The
 successful candidate will be required to provide leadership and management to
 a team of Research Nurses and Clinical Trials Assistants, with the
 expectation of significant engagement in all aspects of trial coordination
 and management, namely the operational, regulatory, risk management and
 financial considerations to ensure safe and effective delivery of the
 portfolio. Additionally, clinical
 cover and direct patient care will be required.
 
 Although,
 chemotherapy competency is not essential, it would be advantageous.
 
 The
 post will be based at St Jamess Institute of Oncology, Level 3 Bexley Wing,
 St James University Hospital Leeds.
 
 
 
  About us
  
 
 
 Research
 is at the heart of our Trust. Leeds Teaching Hospitals is involved in
 research at all levels, developing and trialling new treatments for patients.
 We believe that being involved in cutting-edge research helps us provide
 better care to our patients.
 
 Over
 the next 5 years, we aim to be the best Trust to deliver high-quality
 clinical research and to champion research amongst our staff. We also aim to
 support and grow our world-class clinical infrastructure and assets for
 research and innovation.
 
 We
 have a very proactive Research Academy. It offers an extensive programme of
 education and training tailored to meet the needs of individuals, teams
 involved in clinical research delivery in Health and Social Care.
 
 Our
 five Trust values are part of what make us different. They have been
 developed by our staff. They are:
 
 -
 Patient-centred
 
 -
 Collaborative
 
 -
 Fair
 
 -
 Accountable
 
 -
 Empowered
 
 
 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 be responsible for the co-ordination of the clinical
 research within the Research and Innovation (R&I) department.
 Additionally, where appropriate, they will provide professional, clinical,
 managerial leadership and supervision for the research delivery team. In
 collaboration with the immediate and broader multidisciplinary team (MDT), be
 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.
 
 Working
 effectively and proactively with senior colleagues, the MDT and agreed
 external agencies and collaborative partners, the individual will adhere to
 agreed study pathways and processes to derive accurate and robust data
 capture, of observational and interventional studies, 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 (GCP) 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 be
 instrumental in implementing team objectives to enhance the performance and
 development of the Research Nurses/Midwives, Allied Health Professional(AHPs),
 and Academy for Healthcare Science (AHCS) registered and other research
 delivery staff. They will act as a role model developing the research team,
 ensuring effective management of the department. During exceptional times of
 need, you will contribute to clinical service, as agreed with the Matron for
 the Clinical Service Unit (CSU) and in line with the Trusts escalation
 policy.
 
 This
 unique post requires an enthusiastic and motivated clinical research
 nurse/midwife/AHP or AHCS voluntary (including Clinical Research Practitioner
 (CRP)) or statutory (including Clinical Scientist) registered and any other
 relevant clinical professions to lead a team of clinical research
 nurses/midwives/AHPs and other research delivery team members within R&I.
 The post holder will be a dynamic and motivated individual who will combine
 their managerial responsibilities with the opportunity to further develop
 their own knowledge of the clinical research process and specialist clinical
 knowledge. They will provide leadership and management to Research Delivery
 team As a Senior nurse/midwife/AHP/AHCS you will be expected to provide
 support, clinical supervision and training. Acting in a lead capacity within
 your speciality you will ensure that studies are delivered effectively;
 efficiently and compliant with GCP and other legislative requirements. You
 will also have responsibility for ensuring the completion of study related
 activities across the CSU. Working clinically with the team you will promote
 high standards of both patient care and research practice and facilitate
 appropriate educational and training opportunities. You will also work
 collaboratively across the Trust linking in with other research teams and
 contributing to research delivery workforce developments and work streams.
 The post will cover both the inpatient and outpatient setting with the
 caseload varying in size and complexity according to the trial portfolio. You
 should be able to adopt a flexible approach to the needs of colleagues,
 participants, and external collaborators managing multiple team members and
 representing the research team in both internal and external meetings. You
 must have effective organisational skills and be looking for a new and
 exciting challenge. You should demonstrate the ability to manage your own
 work load and direct the work of others to ensure the team succeeds.
 
 The
 post holder will be required to work alongside academic and 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 be responsible for the co-ordination of the clinical
 research within the Research and Innovation (R&I) department.
 Additionally, where appropriate, they will provide professional, clinical,
 managerial leadership and supervision for the research delivery team. In
 collaboration with the immediate and broader multidisciplinary team (MDT), be
 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.
 
 Working
 effectively and proactively with senior colleagues, the MDT and agreed
 external agencies and collaborative partners, the individual will adhere to
 agreed study pathways and processes to derive accurate and robust data
 capture, of observational and interventional studies, 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 (GCP) 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 be
 instrumental in implementing team objectives to enhance the performance and
 development of the Research Nurses/Midwives, Allied Health Professional(AHPs),
 and Academy for Healthcare Science (AHCS) registered and other research
 delivery staff. They will act as a role model developing the research team,
 ensuring effective management of the department. During exceptional times of
 need, you will contribute to clinical service, as agreed with the Matron for
 the Clinical Service Unit (CSU) and in line with the Trusts escalation
 policy.
 
 This
 unique post requires an enthusiastic and motivated clinical research
 nurse/midwife/AHP or AHCS voluntary (including Clinical Research Practitioner
 (CRP)) or statutory (including Clinical Scientist) registered and any other
 relevant clinical professions to lead a team of clinical research
 nurses/midwives/AHPs and other research delivery team members within R&I.
 The post holder will be a dynamic and motivated individual who will combine
 their managerial responsibilities with the opportunity to further develop
 their own knowledge of the clinical research process and specialist clinical
 knowledge. They will provide leadership and management to Research Delivery
 team As a Senior nurse/midwife/AHP/AHCS you will be expected to provide
 support, clinical supervision and training. Acting in a lead capacity within
 your speciality you will ensure that studies are delivered effectively;
 efficiently and compliant with GCP and other legislative requirements. You
 will also have responsibility for ensuring the completion of study related
 activities across the CSU. Working clinically with the team you will promote
 high standards of both patient care and research practice and facilitate
 appropriate educational and training opportunities. You will also work
 collaboratively across the Trust linking in with other research teams and
 contributing to research delivery workforce developments and work streams.
 The post will cover both the inpatient and outpatient setting with the
 caseload varying in size and complexity according to the trial portfolio. You
 should be able to adopt a flexible approach to the needs of colleagues,
 participants, and external collaborators managing multiple team members and
 representing the research team in both internal and external meetings. You
 must have effective organisational skills and be looking for a new and
 exciting challenge. You should demonstrate the ability to manage your own
 work load and direct the work of others to ensure the team succeeds.
 
 The
 post holder will be required to work alongside academic and 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 Nurse (RN Adult or RN Child or Midwife for Childrens  areas), Midwife or HCPC registered AHP, or AHCS voluntary (including CRP) or  statutory (including  Clinical Scientist)  registered
 
        
        - Degree, or working towards, or equivalent professional experience
 
        
        - Recognised post-registration qualification in speciality
 
        
        - Recognised teaching/assessing qualification
 
        
        - Evidence of effective  professional and leadership development
 
        
      
      
      
    
    
      
        
          Skills & behaviours 
        
      
      
      Essential
      
        
        - Professional and patient  focused
 
        
        - Flexible, adaptable, innovator capable of  lateral thinking
 
        
        - Excellent interpersonal skills
 
        
        - Ability to manage and identify stress in others
 
        
        - Able to deliver feedback effectively
 
        
        - Assertive/self-confident to motivate self and others
 
        
        - Able to work independently and as part of a team
 
        
        - Ability to communicate complicated information effectively within a multi-disciplinary team
 
        
        - Demonstrates influencing and negotiation skills
 
        
        - Displays high motivation and commitment to  success
 
        
        - Demonstrates problem solving and analytical  skills
 
        
        - Ability to prioritise  workload and meet deadlines whilst paying  attention to detail
 
        
        - Ability to work under pressure
 
        
        - Education, training and appraisal skills
 
        
      
      
      
        Desirable
        
          
          - Able to fulfil Occupational Health requirements for the post
 
          
        
      
    
    
      
        
          Experience
        
      
      
      Essential
      
        
        - Extensive post registration experience
 
        
        - Evidence of managing staff and performance management strategies
 
        
        - Evidence of clinical audit, service development or facilitation of change management
 
        
        - Experience of computer database and administration
 
        
      
      
      
        Desirable
        
          
          - Budgetary management experience
 
          
          - Experience of recruitment and selection process
 
          
          - Insight into clinical speciality
 
          
          - Understanding and experience of the research process and clinical research specific issues
 
          
        
      
    
   
  
    
      
        Person Specification
      
    
    
      
      
        
          
            Qualifications
          
        
        
        Essential
        
          
          - Registered Nurse (RN Adult or RN Child or Midwife for Childrens  areas), Midwife or HCPC registered AHP, or AHCS voluntary (including CRP) or  statutory (including  Clinical Scientist)  registered
 
          
          - Degree, or working towards, or equivalent professional experience
 
          
          - Recognised post-registration qualification in speciality
 
          
          - Recognised teaching/assessing qualification
 
          
          - Evidence of effective  professional and leadership development
 
          
        
        
        
      
      
        
          
            Skills & behaviours 
          
        
        
        Essential
        
          
          - Professional and patient  focused
 
          
          - Flexible, adaptable, innovator capable of  lateral thinking
 
          
          - Excellent interpersonal skills
 
          
          - Ability to manage and identify stress in others
 
          
          - Able to deliver feedback effectively
 
          
          - Assertive/self-confident to motivate self and others
 
          
          - Able to work independently and as part of a team
 
          
          - Ability to communicate complicated information effectively within a multi-disciplinary team
 
          
          - Demonstrates influencing and negotiation skills
 
          
          - Displays high motivation and commitment to  success
 
          
          - Demonstrates problem solving and analytical  skills
 
          
          - Ability to prioritise  workload and meet deadlines whilst paying  attention to detail
 
          
          - Ability to work under pressure
 
          
          - Education, training and appraisal skills
 
          
        
        
        
          Desirable
          
            
            - Able to fulfil Occupational Health requirements for the post
 
            
          
        
      
      
        
          
            Experience
          
        
        
        Essential
        
          
          - Extensive post registration experience
 
          
          - Evidence of managing staff and performance management strategies
 
          
          - Evidence of clinical audit, service development or facilitation of change management
 
          
          - Experience of computer database and administration
 
          
        
        
        
          Desirable
          
            
            - Budgetary management experience
 
            
            - Experience of recruitment and selection process
 
            
            - Insight into clinical speciality
 
            
            - Understanding and experience of the research process and clinical research specific issues
 
            
          
        
      
     
   
      
  
    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.
  
  
    
    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).
  
  
    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.
      
      
        
        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).
      
      
        UK Registration
        
          Applicants must have current UK professional registration. For further information please see 
          NHS Careers website (opens in a new window).