Clinical Research Nurse

The purpose of this role is to deliver safe, high-quality

research within and across Suffolk Primary Care. The research nurse will

support the existing Suffolk Primary Care Research team to improve the set-up

time and implementation of clinical research and ultimately patient care. The

role involves using an in-depth knowledge of research protocols and their

application in practice, alongside a working knowledge and compliance with the

local, national and international research regulations. The post holder will

demonstrate effective professional nurse standards, advocacy and

performance.

Excellent communication skills

are essential as is the ability to work independently and as part of a team.

Assess

protocols and advise on safety, regulatory and logistical issues for the set-up

and running of the study/trial to ensure the well-being and safety of patients,

participants and staff.

participants with specialist information regarding their participation,

including risk factors.

a high standard and continuity of care for participants during the research

study, maintaining lines of communication with clinical staff.

Act

as a resource to participants, their families and staff from within the

clinical area, providing information and support; and to act as an effective

referral to other support agencies where necessary.

Achieve

and maintain defined competencies for clinical research to ensure that

capability, skill and knowledge are appropriate for the work undertaken.

within dedicated clinical research teams; ensure ethical and clinical safe

practice.

Undertake,

with appropriate training, interventional treatments directly to participants

according to study/trial protocol and procedures and record the resulting

information.

Take

and process clinical samples (e.g. venepuncture/cannulation) for studies,

coordinate tissue sample collection and dispatch to relevant department or

trial centre as appropriate.

Maintain

clinical skills as appropriate e.g. phlebotomy, vital sign assessment, patient

compliance and ECGs.

Undertake

research-associated laboratory work safely, as required.

Work

at all times as part of the extended multidisciplinary team and maintain

excellent links with staff in primary care regarding the protocol care required

for study/clinical trial participants.

Retrieve

and retain medical records of participants for trial duration.

Conduct

research according to standards and regulations laid down in ICH Good Clinical

Practice and EU Directives, and to the most current guidance relating to

Research Governance and Research Ethics.

Assist

in the provision of background information about potential clinical trials to

obtain approvals from Research Governance and Local Ethics Committees.

Co-ordinate

and manage research within expected timelines.

Work

within and contribute towards the development and review of Standard Operating

Procedures (SOPs) and local policies/procedures for clinical research.

Understand

the requirements of the study protocol and adhere to them

suitable participants eligible for the study/clinical trial, in conjunction

with the site investigator; identify, screen and recruit research participants

using detailed knowledge of the protocols for the designated site specific

groups.

patient/participant documentation for treatment clinics with meticulous

attention to detail and complete accurate records of patient care, maintaining

source data and CRFs in a clearly trackable system, to ensure data validity.

ongoing support, advice and information to patients/participants with regard to

their participation in clinical research in order to facilitate an effective

informed consent process.

Take

informed consent where appropriate; maintain the continuous informed consent of

participants to ensure that the procedures and treatments agreed within the

trial protocol are fulfilled.

Co-ordinate

own case load of participants within the allocated trials, e.g. organising

trialspecific investigations, study treatments, appointments etc. as

necessary.

Meet

with trial sponsors as necessary, providing information requested on trial

participants.

Participate

in research protocol design, development and review: ensure that ethical issues

are addressed and all personnel involved in the study/trial are made aware of

any changes or protocol amendments.

Collect

accurate local data and deliver to clinical trial centres in a timely manner

adhering at all times to the terms of the Data Protection Act

Record

own observations and those of other healthcare professionals, in the trial

database, with accuracy.

Help

to maintain the core entry database; participate in CRF completion, safety

reporting, protocol compliance, monitoring and auditing of clinical

trials.

Attend

relevant local, regional and national meetings related to specific trials.

Assist

with the resolution of data queries; contribute to financial processes of

planning, running and closedown of studies.

Contribute

to study closure and archival preparation

to nurse-led research

Take

opportunities to publish and present findings of research undertaken.

Assist

with the dissemination of research finding.

Suffolk Primary Care (SPC) is a forward-thinking partnership of GP surgeries across Suffolk. Our collaborative approach enables doctors and staff to share resources, ensuring the continued delivery of high-quality healthcare.

We are committed to equal employment opportunities and encourage applications from all qualified individuals.

NHS Pension Scheme

Electric Car Salary Sacrifice Scheme

At SPC, we invest in our staffs professional growth and well-being, fostering a positive work environment that benefits both our team and the communities we serve.

Experience

Qualifications

Essential: - NMC Registered Nurse (Adult Nursing*) - *Paediatric/immunisation experience is an advantage for upcoming studies

Desirable: - ICH GCP training desirable, or a willingness to undertake GCP and associated NIHR training