Clinical Research Nurse

The successful candidate will be working

as part of the Norwich North Primary Care Network research team and based primarily within the dedicated PCN Research Hub at Magdalen Medical Practice, with work across the PCN's member practices and other approved research locations as required. You will be responsible for providing a

safe, efficient and compassionate research based nursing service to our patients.

Job TitleClinical Research Nurse

Reports ToGP Research Lead and Practice Business Manager

Primary Care Network comprises Lawson Road Surgery, Magdalen Medical Practice

and Oak Street Medical Practice. The Clinical Research Nurse will support the

continued development and delivery of the PCNs portfolio of commercial and

non-commercial research. The post will be based primarily within the dedicated

PCN Research Hub at Magdalen Medical Practice, with work across the PCNs

member practices and other approved research locations as required.

The post

holder will: identify, screen and recruit potentially eligible participants;

support the informed-consent process; deliver study-specific clinical

procedures; monitor participants; and ensure that accurate, complete and timely

study documentation is maintained.

closely with Principal Investigators, practice teams, sponsors, research

delivery staff and partner organisations, the post holder will: help ensure

that studies are delivered safely, effectively and in accordance with approved

protocols, Good Clinical Practice, applicable UK legislation and regulatory

undertaken will depend on individual study requirements and will remain within

the post holders professional registration, training, demonstrated competence

and documented delegation by the Principal Investigator.

Occasional flexible working may be required to meet participant and protocol requirements. Any evening, weekend or home-visiting arrangements will be agreed in advance and undertaken in accordance with the practices lone-working and safety procedures

In the performance of the duties outlined in this

Job Description, the post-holder may have access to confidential information

relating to patients and their careers, practice staff and other healthcare

workers. They may also have access to information relating to the Practice as a

business organisation. All such information from any source is to be regarded

as strictly confidential.

Quality and Continuous Improvement (CI)

The post-holder will strive to maintain quality within the Practice, and

Work with the NMC Code of Conduct and scope of

professional conduct

Be responsible for developing and sustaining own

knowledge, clinical skills and professional awareness including clinical

supervision.

Conduct research in accordance with relevant

guidelines such as ICH GCP Guidelines, The Medicines for Human Use (Clinical

Trials) Regulations 2004, as amended; UK Policy Framework for Health and Social

Care Research; current MHRA and HRA guidance; and ICH Good Clinical Practice.

To protect the research participants and quality of

each study.

Attend courses, meetings and conferences as deemed

relevant.

Ensure that the CRN wide standards are maintained

and monitored to improve the quality of care of all those who come in contact

with the service.

Alert other team members to issues of quality and risk.

Assess own performance and take accountability for

own actions, either directly or under supervision

Work effectively with individuals in other agencies

to meet patients needs.

Organise workload to ensure that the interest of

research participants are met.

Prioritise patient safety and accurate data

collection in line with GCP principles

Work within and monitor the standards of care as

defined in the research protocols, policies and procedures of the RDN-EoE to

ensure adherence to and delivery of high quality service.

Support the safe administration of treatments and

drugs given within the context of a clinical trial.

Ensure that trial specific investigations are

undertaken as required by the trial protocol including to undertake clinical

procedures and clinical sampling and processing and shipping of samples as

required

With appropriate training, to take clinical samples

for studies, and ensure the processing and storage and dispatch of biological

samples meets the requirements of the research protocol in order to make

certain that safe handling and quality is assured.

Maintain effective communication with research

participants their relatives/carers and members of the multi-disciplinary teams

Ensure data is recorded accurately and in

accordance with regulatory requirements in appropriate study documentation.

Ensure that all research studies have the necessary

regulatory, ethical, Health Research Authority and organisational approvals in

place before any study-specific activity or participant approach is undertaken.

Provide support to clinical investigators in

obtaining approval and assurances.

Become familiar with each research protocol and its

application in practice including procedures and documentation to ensure safe

and accurate conduct and recording within the study.

To identify, screen and recruit eligible

participants into research studies according to specific protocols and

guidelines.

Co-ordinate recruitment for a local portfolio of

clinical studies across participating sites/practices.

Provide information, education and support to

clinical team members, regarding clinical studies.

Facilitate the informed consent process ensuring

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 filed as required.

disseminate up to date information, protocol amendments etc to personnel

working on research projects.

To be

responsible for monitoring trial data/accrual in clinical studies and uploading

to appropriate systems in a timely manner. Liaise with clinical trial

personnel, as necessary.

To identify

barriers to recruitment to studies and ensure that the Principal Investigator is

aware of them. Identify and implement action/plans as required.

Report all

serious adverse events (SAEs) and suspected unexpected serious adverse

reactions (SUSARs) immediately following appropriate procedures.

Co-coordinate

and assist in the dissemination of research findings internally and externally

Our Research Hub is made up of dedicated GPs, Nurses, GPAs and administrators who work collaboratively to provide the highest standards of patient care. We believe that every member of the team plays a vital role in the success of the Hub and in delivering an exceptional experience for our patients.

We foster a welcoming, supportive and inclusive working environment where colleagues feel valued, respected and encouraged to develop their skills and careers. Teamwork, compassion, professionalism and mutual support are at the heart of everything we do.

If you are looking for a rewarding role within an ambitious, caring and innovative setting, Norwich North Primary Care Network offers an excellent opportunity to develop your career while making a meaningful contribution to your local community.

Knowledge and skills

Experience

Essential: - Relevant recent clinical experience at Band 5 or above; - Experience of collaborating with other agencies; - Working with patients/service users

Qualifications