PCN Research Nurse (Part Time)

• 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.

• 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.

• 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.

• 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.

• 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.

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.