KNOWLEDGE, SKILLS AND EXPERIENCE REQUIRED Qualifications Registered Nurse (Level 1 or 2) (RN Adult for adult areas, RN Child for.....
KNOWLEDGE, SKILLS AND EXPERIENCE REQUIRED Qualifications Registered Nurse (Level 1 or 2) (RN Adult for adult areas, RN Child for childrens areas) Midwife or HCPC registered AHP or Clinical Research Practitioner registered to the Academy for Healthcare Science (AHCS) Recognised post-registration qualification in specialty Recognised teaching/assessing qualification (desirable) Experience Significant post registration experience Experience of computer database and administration Working with a wide range of professionals including medical, nursing and management colleagues Experience of dealing with highly complex situations Experience of providing and receiving highly complex information Skills Ability to communicate effectively within a multi-disciplinary team Time management skills IT skills Knowledge Insight into clinical specialty Insight into clinical research specific issues Standards of professional practice Personal Attributes Professional and patient focused Flexible, adaptable, capable of lateral thinking Excellent interpersonal skills Ability to work independently and as part of a team CORE BEHAVIOUR AND SKILLS Highly developed communication skills Time management skills Organisational skills Research awareness Leadership skills Team player Ability to act professionally at all times Understanding and acting upon change Ability to use own initiative Teaching skills CORE KNOWLEDGE AND UNDERSTANDING Understanding of the local and national nursing research agenda Understanding of relevant National Service Frameworks Awareness of Leeds Teaching Hospitals Trust guidelines and policies Understanding of organisational structures Understanding of the National and local research agenda PRINCIPAL DUTIES AND AREAS OF RESPONSIBILITY Leadership Support the Senior Research Nurse/Midwife/AHP in providing leadership to the research team With the Senior Research Nurse/Midwife help provide clear leadership for the multidisciplinary team ensuring standards are maintained and patient safety assured. Support and inspire staff to provide efficient, effective, safe, quality care to patients Deliver a positive patient experience Promote the building of effective teams and collaboration between teams Anticipate problems and take preventative or mitigating actions, or have contingency plans available Assist in the line management of the research team, including individual and team performance, attendance, management and workforce planning Support the Senior Research Nurse/Midwife/AHP to investigate and respond to accidents, complaints, untoward incidents and other significant events Support the delivery of an effective, safe, quality service within budgetary envelope Raise and respond to concerns with regards to risk, danger, malpractice or wrong doing by following the LTHT Whistleblowing policy and supporting processes. Deputise for Senior Research Nurse/Midwife/AHP in their absence Clinical Research To assist the Senior Research Nurse/Midwife/AHP with the generation, upkeep and distribution of clinical research protocols within the CSU To take delegated responsibility for the coordination and delivery of a portfolio of clinical research studies, ensuring that participants receive high standards of patient focused care in accordance with Leeds Teaching Hospitals Trust guidelines, policies and the trial protocol throughout their participation. To provide on-going advice and information to patients/volunteers with regard to their participation in clinical research in order to facilitate effective informed consent and to maintain a supportive role throughout the trial. Ensure that you obtain and maintain high levels of understanding in relation to the clinical and delivery of the research studies that you support. To assist in the assessment of patients/volunteers for eligibility for research and monitoring of their condition throughout their participation. To coordinate trial investigations, treatments and procedures according to trial protocols and professional body the person in post belongs to. Help obtain ethical and local approval for projects. Liaise with, and prepare submissions, for the Trust Research & Innovation department (R&I) for new clinical trials and provide annual updates of trial activity Word processing standard letters and other communications as appropriate To accurately collate data on relevant trial pro-formas within a pre-determined timeframe and respond to data queries. To liaise with representatives from pharmaceutical commercial companies and prepare data for monitoring by these representatives. To accurately and promptly report and document Serious Adverse Events, or Reactions, to the relevant clinician, Sponsor and authorities within the required timelines, ensuring any interventions or modifications are carried out. To accurately report and document Adverse Events, or Reactions, and ensure any modifications required as a consequence are carried out. Assist in the preparation of results of research for presentation as posters or scientific presentation To perform clinical tasks when required for research purposes. (Included venepuncture and central line access for Registered Nurse/Midwife) To process, store and despatch blood, urine and other biological samples according to trial protocols and Trust policies and guidelines. To assist other members of the team in providing when necessary 24 hour support and advice for Phase I, II, III and pharmacokinetic studies For registered Nurses/Midwifes: To safely administer trial medications in adherence to Trust policies and research protocols. To educate patients and their carers with regards to trial medications particularly when medications require home self-administration Clinical Service and Professional Responsibilities To work as part of the multidisciplinary team and contribute to the on-going development of the department. To be responsible for maintaining strong relationships and positive communication channels with other key personnel and internal and external partner departments. To take an active role in education and training of various groups with regards to specific trial requirements and clinical research in general. To take an active role in regional research networks. To act in an advisory capacity for regional or national groups if required. To fulfil the requirements as directed by the registration body the person in post belongs to (for example: Nursing and Midwifery Council or Health and Care Professions Council to maintain and revalidate registration) To observe the confidentiality of patient information at all times, in accordance with the Data Protection Act and local information governance policy. To be conversant with cardiac arrest, major incident and fire procedures as they relate to your local clinical area and the wider Trust. To be conversant with and adhere to all clinical protocols, local departmental and Trust protocols. Undertake duties on other wards or departments as and when required by service demands or patient need. To be actively involved in any Patient and Public Involvement initiatives Act in such a way that safeguards the health and wellbeing of children and vulnerable adults at all times. Is familiar with and adheres to, the LTHT safeguarding policies Actively promote and use The Leeds Improvement Method to improve quality and safety of the service. Maintain an active knowledge of the Trusts clinical and research IT systems (in particular EDGE) by actively supporting their use. Ability to deal with highly complex, contentious and sensitive information on a daily basis Provide and receive highly complex information Personal Education, Training and Development Undertake mandatory and priority training within the required timescales To keep up to date with departmental, Trust, NHS and EU developments for the implementation of clinical research. To keep up to date with current and potential research and information relevant to the care of patients in the clinical area. To attend courses as deemed relevant and to attend meetings and conferences as appropriate. To be responsible for developing and sustaining own knowledge, clinical skills and professional awareness. Participate in own and others appraisals. Supports and keeps up-to date with the Trusts Clinical Research Forum. Actively participate in the Trusts development of the clinical research service. Actively support the education and training developmental needs of others and those of junior staff. Staff Management and Development To act as a resource and role model. To facilitate and maintain effective communication within the research team. This is not an exhaustive list of roles and responsibilities and may be subject to change with professional and service developments.