Research Nurse

NHS; Witney; On-site; GBP 30,000 - 40,000; Full time

Job summary

A progressive NHS practice in Witney is seeking a skilled Research Nurse to join their clinical research team. The role involves delivering and supporting clinical trials, recruiting patients, and ensuring compliance with protocols. Ideal candidates will have nursing experience, a keen interest in research, and strong clinical skills. This position offers meaningful patient interaction and collaboration within a multidisciplinary team, contributing to vital studies that impact healthcare delivery.

Qualifications

• Post-registration clinical nursing experience within the NHS.
• Experience delivering patient-centred care.
• Experience in clinical research or clinical trials.

Responsibilities

• Deliver and coordinate clinical research studies according to protocols.
• Recruit, consent, and follow up with study participants.
• Support the nursing team with routine clinical duties.

Skills

Clinical skills relevant to patient assessment

Effective communication skills

Organisational skills

Ability to work autonomously

Attention to detail

Education

Degree in Nursing or related health/science field

Registered Nurse with current NMC registration

Completed GCP certification

Job description

Eynsham Medical Group is seeking a skilled and motivatedResearch Nurseto join our growing clinical research team. You willpredominantly work as a researchnurse, delivering and supporting clinical trials and observational studies in primary care. During quieter research periods, you will also be expected tosupport the wider nursing teamwith routine clinical duties, providing flexibility and helping ensure smooth patient care.

This is an exciting opportunity for a nurse with research experienceor a strong interest in clinical researchto contribute to meaningful studies and work closely with patients and a supportive multidisciplinary team.

Main duties of the job

• Deliver and coordinate clinical research studies in accordance with trial protocols and Good Clinical Practice (GCP) guidelines
• Recruit, consent, and follow up with study participants
• Collect, process, and manage clinical samples and data accurately
• Liaise with research sponsors, investigators, and the wider clinical team
• Support the nursing team with routine clinical duties during quieter research periods
• Ensure compliance with all regulatory and ethical requirements
• Deliver and coordinate clinical research studies in accordance with trial protocols and Good Clinical Practice (GCP) guidelines
• Recruit, consent, and follow up with study participants
• Collect, process, and manage clinical samples and data accurately
• Liaise with research sponsors, investigators, and the wider clinical team
• Support the nursing team with routine clinical duties during quieter research periods
• Ensure compliance with all regulatory and ethical requirements

About us

Eynsham Medical Group is a progressive, patient-centred NHS practice serving 15,000 people across its Eynsham and Long Hanborough sites. As a teaching and training practice, it supports medical students, GP trainees, and multidisciplinary learners, fostering a culture of collaboration and high-quality care. Research is firmly embedded in daily work, supported by strong links with the NIHR Thames Valley & South Midlands Clinical Research Network. The practice contributes to major national studies, including vaccine trials and projects in chronic disease and public health. For research nurses, it offers a supportive, development-focused environment with meaningful patient contact and opportunities to influence NHS care.

Job responsibilities

The Research Nurse will support the development, delivery, and coordination of clinical research activity within Eynsham Medical Practice. You will work closely with the practice team, Clinical Research Network (CRN), and study sponsors to recruit, assess, and care for participants in NIHR and other approved research studies. You will play an essential role in embedding research into routine primary care and ensuring high standards of patientcentred research delivery.

Key Responsibilities

Research Delivery

• Support identification and feasibility of suitable research studies for the practice.

Screen and recruit eligible patients according to study protocols and ethical guidelines.

Obtain and document informed consent from participants.

Implement study procedures safely and accurately in line with Good Clinical Practice (GCP) and study protocols.

Collect and record data and samples in accordance with protocol requirements and standard operating procedures (SOPs).

Maintain research documentation, case report forms, and regulatory files.

Clinical & Patient-Cantered Work

Provide clinical assessments and basic procedures required by the study (e.g., observations, venepuncture where trained).

Act as the main point of contact for research participants, offering support and clear communication throughout their involvement.

Work collaboratively with GPs, nurses, healthcare assistants, and admin staff to coordinate participant care and research activity.

Governance & Compliance

• Ensure compliance with research governance frameworks, Data Protection, and local policies.
• Highlight and report any deviations, safety issues, or adverse events to study sponsors and practice leads.
• Maintain confidentiality, consent records, and ethical standards at all times.
• Education & Promotion
• Engage with the practice team to raise awareness of current research and encourage patient participation.
• Provide information to patients and staff about the importance, benefits, and requirements of research participation.
• Attend relevant meetings, training, and research forums as required.

Professional Duties

• Maintain registration with the Nursing and Midwifery Council (NMC).
• Uphold NHS and practice standards of professionalism, including the NMC Code of Professional Conduct.
• Participate in mandatory training and continuous professional development.
• Actively contribute to practice quality improvement and audit where relevant.

Key Working Relationships

• Practice Partners & GPs
• Clinical Research Network staff
• Study sponsors and external research teams

Person Specification

Experience

• Post-registration clinical nursing experience within the NHS or equivalent setting.
• Experience delivering patient-centred care with high standards of safety and quality.
• Experience maintaining accurate clinical records and documenting care.
• Excellent clinical skills relevant to patient assessment and monitoring.
• Ability to work autonomously while following study protocols precisely.
• Strong organisational skills and ability to manage multiple studies or tasks.
• Effective communication skills, including the ability to explain research to patients.
• High attention to detail for accurate data collection and documentation.
• Ability to work collaboratively across multidisciplinary and research teams.
• Ability to handle sensitive conversations regarding consent and study participation.
• Competence in using IT systems, email, databases, and electronic health records.
• Previous experience working in clinical research, clinical trials, or audit.
• Experience recruiting participants to studies.
• Experience collecting and handling study samples (e.g., bloods, swabs).
• Experience working within multidisciplinary teams.
• Venepuncture and cannulation skills (or willingness to undertake training).
• Experience in processing biological samples
• Ability to mentor junior staff or students.

Qualifications

• Registered Nurse (Adult/Child/Mental Health) with current NMC registration.
• Evidence of continuing professional development (CPD).
• Completed GCP certification
• Good understanding of Good Clinical Practice (GCP) and willingness to undertake GCP training.
• Post-registration qualification in research, clinical trials, or a relevant speciality.
• Degree in Nursing or related health/science field.
• Training in informed consent processes.

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.