Clinical Research Nurse

Queen Square Medical Practice

Information:

This job is now closed

Job summary

Clinical Research Nurse required for Queen Square Medical Practice, Lancaster.

We are a proudly independent, innovative, friendly, research active practice, with a practice population of 15,000 patients . We are a dynamic team of doctors, practitioners and nurses constantly developing our service.

The Research Nurse role is vital and varied and the successful candidate would ideally be able to undertake a range of core clinical competencies as identified in the job description.

We are looking for that exceptional Nurse who is driven to ensure excellent care to our patients.

Main duties of the job

The Research Nurse involves recruiting patients into a wide range of National Institute of Health Research (NIHR) studies within primary care, receiving informed consent, conducting study procedures 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.

About us

Queen Square Medical Practice is a proudly independent, vibrant, friendly, and innovative practice. We have 9 GP partners and 3 associate GP's; nurse, pharmacist and paramedic practitioners who are supported by an excellent multi skilled nursing team and admin team. The management team work closely together.

In addition to normal GP services we run Travel, Sexual Health, Gynaecology, Fertility, Dermatology clinics. We are also an award winning lead research practice working in close alliance with other research active practices across the Morecambe Bay CCG footprint. All this offers lots of variety and an opportunity for growth and development to apply new skills.

We believe in strong clinical and management leadership with a clear emphasis on teamwork and adaptability to ensure a happy working environment and good work-life balance.

We work closely with local practices and other community partners whilst maintaining our independence. Our size and independence means we can offer a flexible supportive working environment in which staff have opportunities to develop and try new skills.

Join us and try something new!

Date posted

15 September 2021

Pay scheme

Other

Salary

Depending on experience

Contract

Permanent

Working pattern

Part-time

Reference number

A1352-21-1871

Job locations

2 Queen Square

Lancaster

Lancashire

LA1 1RP


Job description

Job responsibilities

Job Title: Research Nurse

This post is funded via the National Institute of Clinical Research (NIHR) Network, North West Coast. Queen Square Medical Practice will host the post holder

Salary: Band 5 / 6 dependent on experience

Hours: 16hrs per week

Reporting to: Research Development Nurse and Practice Director

Base: Queen Square Medical Practice, Lancaster

Duties and Responsibilities

Clinical

You must be a Registered Nurse (with valid NMC) and possess excellent organisational, communication and interpersonal skills. Previous experience is desirable but not essential as training can be provided.

Contributes to the planning and the logistics 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 relatives/carers and members of the multi-disciplinary team

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 GP

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

Responsible for the receipt and storage of study medication and drug accountability together with the Principle 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 in order to make certain that safe handling and quality is assured

Be willing to undertake further training required of the role as and when identified and required to develop personal competencies and role development.

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

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 different levels of understanding, cultural background and preferred ways of communicating

Participate in research, practice and other multidisciplinary meetings

Personal and people development

Uphold the Nursing and Midwifery Councils (NMC) code of Conduct at all times and maintain an up to date professional profile and NMC registration.

Actively promote the workplace as a learning environment

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 well being of patients are protected, consistent with the principles of Good Clinical Practice (GCP)

Be familiar and adhere to local 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 mandatory training either online or in person. 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

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

Observes the confidentiality of patient information at all times, in accordance with the Data Protection Act (1998), Caldicott and GDPR regulations.

Maintain confidentiality with regard to research data, and follow research and ethics protocols.

Clinical and corporate governance/quality assurance

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

We are an equal opportunities employer and welcome all applications irrespective age, disability, gender, sexual orientation, race or religion. All sites are smoke free.

Disclosure/criminal record

This post is subject to Disclosure and Barring Service (DBS) check.

Job description

Job responsibilities

Job Title: Research Nurse

This post is funded via the National Institute of Clinical Research (NIHR) Network, North West Coast. Queen Square Medical Practice will host the post holder

Salary: Band 5 / 6 dependent on experience

Hours: 16hrs per week

Reporting to: Research Development Nurse and Practice Director

Base: Queen Square Medical Practice, Lancaster

Duties and Responsibilities

Clinical

You must be a Registered Nurse (with valid NMC) and possess excellent organisational, communication and interpersonal skills. Previous experience is desirable but not essential as training can be provided.

Contributes to the planning and the logistics 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 relatives/carers and members of the multi-disciplinary team

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 GP

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

Responsible for the receipt and storage of study medication and drug accountability together with the Principle 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 in order to make certain that safe handling and quality is assured

Be willing to undertake further training required of the role as and when identified and required to develop personal competencies and role development.

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

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 different levels of understanding, cultural background and preferred ways of communicating

Participate in research, practice and other multidisciplinary meetings

Personal and people development

Uphold the Nursing and Midwifery Councils (NMC) code of Conduct at all times and maintain an up to date professional profile and NMC registration.

Actively promote the workplace as a learning environment

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 well being of patients are protected, consistent with the principles of Good Clinical Practice (GCP)

Be familiar and adhere to local 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 mandatory training either online or in person. 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

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

Observes the confidentiality of patient information at all times, in accordance with the Data Protection Act (1998), Caldicott and GDPR regulations.

Maintain confidentiality with regard to research data, and follow research and ethics protocols.

Clinical and corporate governance/quality assurance

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

We are an equal opportunities employer and welcome all applications irrespective age, disability, gender, sexual orientation, race or religion. All sites are smoke free.

Disclosure/criminal record

This post is subject to Disclosure and Barring Service (DBS) check.

Person Specification

Qualifications

Essential

  • 1st Level Nurse with valid NMC registration.
Person Specification

Qualifications

Essential

  • 1st Level Nurse with valid NMC registration.

UK Registration

Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).

Additional information

UK Registration

Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).

Employer details

Employer name

Queen Square Medical Practice

Address

2 Queen Square

Lancaster

Lancashire

LA1 1RP


Employer's website

https://www.queensquare.org/ (Opens in a new tab)

Employer details

Employer name

Queen Square Medical Practice

Address

2 Queen Square

Lancaster

Lancashire

LA1 1RP


Employer's website

https://www.queensquare.org/ (Opens in a new tab)

For questions about the job, contact:

Research Nurse

Elley Sowerby

eleanor.sowerby@nhs.net

01524843333

Date posted

15 September 2021

Pay scheme

Other

Salary

Depending on experience

Contract

Permanent

Working pattern

Part-time

Reference number

A1352-21-1871

Job locations

2 Queen Square

Lancaster

Lancashire

LA1 1RP


Supporting documents

Privacy notice

Queen Square Medical Practice's privacy notice (opens in a new tab)