Harbourside Family Practice

PCN Research Nurse (Part Time)

Harbourside Family Practice View all jobs


North East England
Temporary
Registered Nurse/RN
GBP 16 - 24 per year

Posted 3 hour(s) ago

Reference: 2481186


Job summary

Gordano Valley Primary Care Network (PCN) is seeking an enthusiastic and motivated Research Nurse to support the delivery and expansion of high-quality clinical research across our four member practices:

  • Clevedon Medical Centre
  • Harbourside Family Practice
  • Heywood Family Practice
  • Portishead Medical Group

This is an exciting opportunity to contribute to the growth of research within primary care and to improve patient outcomes through participation in innovative studies. The successful candidate will work alongside PCN Research Leads to support the delivery of a diverse portfolio of research projects, including observational studies, interventional trials, and studies involving investigational medicinal products.

Salary will be commensurate with previous clinical research experience, relevant certifications, and level of responsibility within the role.

Working hours are anticipated to be around 18 to 22 hours per week and will be agreed with the successful candidate as part of the overall remuneration package.

This role is offered on a 12-month fixed-term contract, with scope for extension.

We are unable to offer visa sponsorship for this role.

Main duties of the job

The post holder will play a key role in identifying, recruiting, assessing, and supporting research participants throughout their research journey, ensuring studies are delivered safely, efficiently, and in accordance with regulatory requirements and Good Clinical Practice (GCP).

About us

Why Join Gordano Valley PCN?

Join a growing research team at the forefront of primary care innovation. As a leading PCN in neighbourhood working, we collaborate with our local Commercial Research Delivery Partner, with one of our practices already delivering high-quality commercial research. This role offers the opportunity to make a meaningful contribution to patient care through research that informs future healthcare, while developing your skills and expertise in a supportive, collaborative environment.

Details
Date posted

09 November 2026

Pay scheme

Other

Salary

£16.40 to £24.78 an hour Band 5/6 equivalent depending on experience

Contract

Fixed term

Duration

12 months

Working pattern

Part-time

Reference number

A0356-26-0014

Job locations

2 Haven View

Portishead

Bristol

BS20 7QA

United Kingdom


Clevedon Medical Centre

Old Street

CLEVEDON

Avon

BS21 6DG

United Kingdom


Portishead Medical Group

Victoria Square

Portishead

BRISTOL

BS20 6AQ

United Kingdom


Heywood Family Practice

1 Lodway Gardens

Pill

BRISTOL

BS20 0DL

United Kingdom


Job description
Job responsibilities

Main Duties and Responsibilities

Research Delivery

  • Identify, screen, recruit and consent eligible participants in accordance with study protocols and delegated responsibilities.
  • Coordinate and undertake study visits, assessments and follow-up appointments.
  • Monitor participants throughout the duration of research studies, ensuring their safety, wellbeing and comfort at all times.
  • Promote patient-centred care and provide participants with clear information and support throughout their involvement in research.
  • Escalate clinical concerns promptly and report adverse events in accordance with study protocols and regulatory requirements.

Clinical Responsibilities

Undertake study-related procedures as delegated, including but not limited to:

  • Measurement of vital signs.
  • Venepuncture and collection of blood, urine and other samples.
  • ECG recording.
  • Collection and documentation of medical histories.
  • Administration of study medications where appropriately trained and delegated.
  • Participant assessment, care planning and ongoing clinical monitoring.

Research Administration and Governance

  • Maintain accurate, contemporaneous and complete source documentation and study records.
  • Complete database entries, case report forms and electronic data capture systems in a timely manner.
  • Ensure compliance with Good Clinical Practice (ICH-GCP), UK regulations, GDPR and local Standard Operating Procedures (SOPs).
  • Maintain Investigator Site Files, study documentation and essential records.
  • Support safety reporting activities and resolution of data queries.
  • Maintain an up-to-date training portfolio and evidence of competency.

Study Management and Development

  • Assist with the feasibility, set-up and implementation of new research studies across the PCN.
  • Support recruitment planning and contribute to meeting study recruitment targets.
  • Coordinate appointments, investigations, sample handling and participant follow-up activities.
  • Work collaboratively with study sponsors, Clinical Research Networks, Contract Research Organisations (CROs) and external partners.
  • Attend study initiation visits, investigator meetings and research team meetings as required.
  • Support the promotion of research opportunities within the PCN and wider community.

Team Working

  • Work independently while maintaining close collaboration with GPs, practice teams, research leads and wider multidisciplinary colleagues.
  • Develop positive relationships with participants, colleagues and external research partners.
  • Contribute to a culture of continuous improvement and excellence in research delivery.
  • Effectively prioritise workload and manage multiple studies simultaneously.
Job description
Job responsibilities

Main Duties and Responsibilities

Research Delivery

  • Identify, screen, recruit and consent eligible participants in accordance with study protocols and delegated responsibilities.
  • Coordinate and undertake study visits, assessments and follow-up appointments.
  • Monitor participants throughout the duration of research studies, ensuring their safety, wellbeing and comfort at all times.
  • Promote patient-centred care and provide participants with clear information and support throughout their involvement in research.
  • Escalate clinical concerns promptly and report adverse events in accordance with study protocols and regulatory requirements.

Clinical Responsibilities

Undertake study-related procedures as delegated, including but not limited to:

  • Measurement of vital signs.
  • Venepuncture and collection of blood, urine and other samples.
  • ECG recording.
  • Collection and documentation of medical histories.
  • Administration of study medications where appropriately trained and delegated.
  • Participant assessment, care planning and ongoing clinical monitoring.

Research Administration and Governance

  • Maintain accurate, contemporaneous and complete source documentation and study records.
  • Complete database entries, case report forms and electronic data capture systems in a timely manner.
  • Ensure compliance with Good Clinical Practice (ICH-GCP), UK regulations, GDPR and local Standard Operating Procedures (SOPs).
  • Maintain Investigator Site Files, study documentation and essential records.
  • Support safety reporting activities and resolution of data queries.
  • Maintain an up-to-date training portfolio and evidence of competency.

Study Management and Development

  • Assist with the feasibility, set-up and implementation of new research studies across the PCN.
  • Support recruitment planning and contribute to meeting study recruitment targets.
  • Coordinate appointments, investigations, sample handling and participant follow-up activities.
  • Work collaboratively with study sponsors, Clinical Research Networks, Contract Research Organisations (CROs) and external partners.
  • Attend study initiation visits, investigator meetings and research team meetings as required.
  • Support the promotion of research opportunities within the PCN and wider community.

Team Working

  • Work independently while maintaining close collaboration with GPs, practice teams, research leads and wider multidisciplinary colleagues.
  • Develop positive relationships with participants, colleagues and external research partners.
  • Contribute to a culture of continuous improvement and excellence in research delivery.
  • Effectively prioritise workload and manage multiple studies simultaneously.
Person Specification
Qualifications
Essential
  • Registered Nurse with current NMC registration.
  • Full UK driving licence and ability to travel between PCN sites.
Desirable
  • Good Clinical Practice (GCP) certification.
Experience
Essential
  • Experience working in a clinical healthcare environment.
  • Excellent communication and interpersonal skills.
  • Strong organisational skills and attention to detail.
  • Ability to work independently and as part of a multidisciplinary team.
  • Competent IT skills, including electronic patient records and data management systems.
Desirable
  • Previous research nursing experience.
  • Experience of participant recruitment and informed consent processes.
  • Knowledge of research governance and regulatory requirements.
  • Experience within primary care settings.
  • Experience working with clinical trial databases and electronic data capture systems.
Person Specification
Qualifications
Essential
  • Registered Nurse with current NMC registration.
  • Full UK driving licence and ability to travel between PCN sites.
Desirable
  • Good Clinical Practice (GCP) certification.
Experience
Essential
  • Experience working in a clinical healthcare environment.
  • Excellent communication and interpersonal skills.
  • Strong organisational skills and attention to detail.
  • Ability to work independently and as part of a multidisciplinary team.
  • Competent IT skills, including electronic patient records and data management systems.
Desirable
  • Previous research nursing experience.
  • Experience of participant recruitment and informed consent processes.
  • Knowledge of research governance and regulatory requirements.
  • Experience within primary care settings.
  • Experience working with clinical trial databases and electronic data capture systems.
Disclosure and Barring Service Check

This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.

UK Registration

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

Additional information
Disclosure and Barring Service Check

This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.

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

Harbourside Family Practice

Address

2 Haven View

Portishead

Bristol

BS20 7QA

United Kingdom


Employer's website

https://www.harboursidefmp.nhs.uk/ (Opens in a new tab)


Employer details
Employer name

Harbourside Family Practice

Address

2 Haven View

Portishead

Bristol

BS20 7QA

United Kingdom


Employer's website

https://www.harboursidefmp.nhs.uk/ (Opens in a new tab)