Research Nurse/ Research Development Nurse inLancaster inLancaster PUBLISHED 2 DEC 2023

• Job Title: Research Nurse/Research Development Nurse

Hours: Up to 36.5 hours per week #2 21.5 hours available form December '24, increasing to 36.5 hours from February '25

Tenure: Permanent, job share will be considered #3

Reporting to: Research Development Nurse Lead and Practice Director

Base: Queen Square medical Practice Lancaster

#1 Queen Square Medical Practice do not operate Agenda for Change, however pay is aligned to AfC pay banding.

#2 Due to staffing changes and funding arrangements there will be an initial offer of 21.5 hours per week from December '24, increasing to 36.5 hours per week , from February '25. A job share role will be considered.

#3 This post is funded via the Research Delivery Networks (Formerly the National Institute of Clinical Research (NIHR) Network Northwest Coast. Queen Square medical practice will host the post holder.

Duties and responsibilities

Clinical

Contributes to the planning and the coordination of research trials adhering to the programme of care as defined by the research protocol

To be familiar with all relevant study protocols and amendments

To ensure data is recorded accurately and in accordance with regulatory requirements in appropriate study documentation

To maintain effective communication with research participants their relative/carers and members of the multi-disciplinary teams

Acts in the best interests of the research subjects to ensure their rights are upheld

To support the safe administration of treatments and drugs given within the context of a clinical trial

Record and report any adverse events to the lead research GP

Assist in recruitment, consenting, follow up and data entry during the period of the trial

Participate in the pre-study screening of subjects

Responsible for the receipt and storage of study medication and drug accountability together with the principal investigator

Ensure safe storage of clinical supplies as per trial protocol

Ensure equipment is maintained and appropriate action taken in the event of equipment failure

With appropriate training, to take clinical samples for studies, and ensure the processing and storage and despatch of biological samples meets the requirements of the research protocol to make certain that safe handling and quality is assured

Organise own work on a day-to-day basis

Be willing to undertake further training required for the role as and when identified and required to develop personal competencies and further role development. Identify, and manage as appropriate, treatment plans for patients at risk of developing a long-term condition

Support patients to adopt health promotion strategies that encourage them to live healthily, and apply principles of self-care

Prioritise health problems and intervene appropriately to assist the patient in complex, urgent or emergency situations, including initiation of effective emergency care

Work with patients to support adherence to prescribed treatments.

Communication

To facilitate the informed consent process ensuring the following is accounted for:

The patient (and significant others) fully understands the nature of the clinical trial.

The patient is aware that entry into the trial is voluntary, and they can withdraw at any point without prejudice

The patient is aware of any extra procedures required by the trial

The consent form is completed accurately, and files as required

• Liaise with other research nurses and colleagues in the local Clinical Research Network (CRN).

• Maintain effective communication with individuals and groups within the practice environment and with external stakeholders

• Communicate effectively with patients and carers, recognising the need for alternative methods of communication to overcome diverse levels of understanding, cultural background, and preferred ways of communicating

• Participate in multidisciplinary meetings

Personal and professional development

• Always uphold the Nursing and Midwifery Councils (NMC) code of Conduct and maintain an up-to-date professional profile and NMC registration.

• Actively promote the workplace as a learning environment

• Contribute and participate in the development of local guidelines, protocols, and standards

• The above list of duties and responsibilities is not intended to be fully comprehensive and may be amended to take account of changing circumstances or requirements following consultation with the post holder

Health, safety and security

• The rights, safety and wellbeing of patients are protected, consistent with the principles of good clinical practice

• Use the personal security systems within the workplace according to practice guidelines

• Identify the risks involved in work activities and undertake them in a way that manages the risks

• Be familiar and adhere to guidance on infection control

• Know the health and safety policies and procedures within the workplace, including fire procedures, maintaining documentation, and monitoring and maintaining of equipment within your area of responsibility.
• Each member of staff has a statutory obligation to attend a fire lecture each year. It is the responsibility of each member of staff to ensure that they comply with this requirement

• Be aware of statutory child health procedures and statutory local guidance and referral criteria

• Use the computer monitor safely

Equality and diversity

• Act in a way that recognises the importance of peoples rights, interpreting them in a way that is consistent with procedures

• Respect the privacy, dignity, needs and beliefs of patients

Confidentiality

• Always observes the confidentiality of patient information, in accordance with the Data Protection Act (1998), Caldicott and GDPR regulations.
• Maintain confidentiality regarding research data and follow research and ethics protocols.

Clinical and Corporate governance/quality

• All employees are expected to comply with the clinical and corporate governance arrangements of the practice.

• Contribute to clinical governance at a level appropriate to the post holders knowledge and experience

• Works within the range of research guidelines, ethical principles, and protocols, whilst adhering to organisational policies and procedures

Information processes

• Access and record patient information using information technology

• Competent in recording trial information into the case report file

• Maintenance of site research files in good order.

Clinical negligence

• Practice indemnity will cover that part of your work, which results from your contract of employment. You are advised to make other arrangements to protect yourself in respect of work deemed to be outside of your contract

Harrassment and bullying

• The practice condemns all forms of harassment and bullying and is actively seeking to promote a workplace where employees are treated with dignity, respect and without bias.

Outside employment/interests

• If you have other work or outside interests, this must not conflict with your duties and responsibilities of your attendance for work as an employee

Equal opportunities

• In all the foregoing text any reference to one gender whether direct or implied equally includes the opposite gender unless specifically stated to be otherwise

Disclosure/criminal record

• This post will be subject to an enhanced disclosure under the CRB

Research Nurse/Research Development Nurse required for Queen Square Medical Practice, Lancaster.

Queen Square Medical practice offer the highest standard of healthcare to our patients in Lancaster, Caton and surrounding area.

We are a proudly independent, innovative, friendly, research active practice, with a practice population of 15,500 patients . We are a dynamic team of doctors, practitioners and nurses constantly developing our service.

Clinical research is vital to the progression of understanding, prevention and treatment of all illnesses, viruses and diseases.

We are looking for that exceptional Nurse who is driven to ensure excellent care to our patients. We are extremely proud to be an award-winning Research Practice.

The Research Nurse involves recruiting participants into a wide range of National Institute of Health Research (NIHR) studies within primary care, receiving informed consent, conducting study procedures and the colloection of baseline and follow up data. You will work collaboratively with the whole practice team to help embed and support research activity.

Experience would be desirable in practice/community nursing. Ideally you will have some knowledge of Asthma, Diabetes, CHD, Family Planning and cytology.