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Clinical Research Nurse

3 months ago

Huntingdon, Cambridgeshire, United Kingdom North West Anglia NHS Foundation Trust Full time

Position Overview

The North West Anglia NHS Foundation Trust is excited to present a unique opportunity for a dedicated registered nurse to become a vital member of our esteemed E&M Team. This role will primarily concentrate on research initiatives within the fields of cardiology and respiratory care, and we encourage applications from individuals with relevant experience in these specialties. Depending on workload, positions may be available at band 5/6 development or band 6 level, contingent upon demonstrable essential experience. There is potential for advancement to a band 6 role, based on the attainment of necessary clinical research competencies.

A solid nursing background in either clinical practice or research is a prerequisite. Successful candidates will play a crucial role in delivering high-quality research outcomes. The position will be based at our facilities, with a requirement for cross-site collaboration.

Your research expertise and knowledge gained through recognized continuing professional development (CPD) will significantly enhance our research team, which comprises both clinical and non-clinical personnel, local healthcare providers, and relevant research networks dedicated to developing and executing high-quality research activities.

You will collaborate closely with local Research and Development (R&D) members to evaluate capacity and capability for research, working alongside research teams to inform potential participants about suitable projects.

While training will be provided, all candidates must familiarize themselves with Good Clinical Practice (GCP) standards.

Key Responsibilities

In this role, you will effectively engage with our clinical research team across the Trust, supporting staff and managing a caseload of patients.

You will ensure effective communication with patients, caregivers, and healthcare professionals to facilitate service delivery. Your responsibilities will include providing research information to patients and their families, serving as a resource and support for them, and clarifying practical aspects of clinical research.

Facilitating the informed consent process is a critical aspect of your role, ensuring compliance with Good Clinical Practice (GCP) and that patients and their families fully comprehend the nature of the research.

A primary responsibility will be to ensure that study-specific investigations are conducted as outlined in the research protocol, safeguarding the well-being of study participants.

As part of your research duties, you will monitor treatment toxicity and side effects, making necessary adjustments to treatment as dictated by the research protocol. You will coordinate the collection of blood and other research samples required for clinical research, ensuring their safe and appropriate storage in collaboration with local clinical and nursing teams, phlebotomy, and laboratory staff.

We encourage you to reach out for an informal discussion about the role or to arrange a visit to gain further insights into the responsibilities involved.

About Our Organization

We are committed to promoting diversity and inclusivity within our workforce and warmly welcome applications from individuals of all backgrounds, particularly those from disabled, Black, Asian, and Minority Ethnic (BAME) communities, as well as candidates from our local area.

In line with our commitment to supporting our employees, we offer a comprehensive range of benefits, including:

  • Generous annual leave starting at 27 days, increasing to 29 days after five years of service and 33 days after ten years of service, in addition to national Bank Holidays (pro-rata for part-time staff);
  • Membership in the NHS Pension Scheme;
  • Flexible working arrangements;
  • Enhanced pay rates for unsociable hours, including night shifts, weekends, and bank holidays;
  • Opportunities for professional development and training to facilitate career progression;
  • Wellbeing support and initiatives to foster a healthy work environment;
  • Access to our in-house physiotherapy services;
  • On-site canteens offering subsidized meals;
  • Subsidized staff parking (currently free);
  • Complimentary bus travel to and from work within designated areas.

We strive to cultivate a supportive and inclusive workplace where employees feel valued and empowered to excel in their roles. Join us in making a positive impact in our community.

Job Responsibilities

For further details regarding this role, please refer to the attached comprehensive Job Description and Person Specification.

Qualifications and Experience

Essential

  • NMC registered Nurse with experience in clinical research or acute nursing.
  • Evidence of relevant post-registration qualifications in acute nursing and/or research.
  • Knowledge of Research Design Networks.
  • Evidence of continuous personal and professional development.
  • Leadership qualification or a willingness to pursue one.

Experience

Essential

  • Extensive post-registration experience in clinical settings within the Emergency and Medicine Division and/or Research.
  • Collaboration with external agencies.
  • Demonstrated experience at a band 6 or Senior Band 5 level.
  • Ability to explain complex concepts to patients.
  • Proficiency in using MS Office and Excel spreadsheets.

Desirable

  • Direct experience in initiating and conducting research projects.
  • Familiarity with HR policies and procedures.
  • Capability to assess the competence of others.

Key Skills

Essential

  • Demonstrated extensive clinical skills across various disciplines.
  • Experience working effectively both independently and as part of a team.
  • Strong organizational abilities.
  • Excellent oral and written communication skills.
  • Meticulous and accurate data collection skills.
  • Commitment to the principles of clinical governance and supervision.
  • Phlebotomy skills.

Desirable

  • Proficiency in report writing and presentation skills.
  • Competence with database applications and data presentation.

Knowledge

Essential

  • Understanding of ICH Good Clinical Practice (GCP).
  • Evidence of ongoing professional and academic development through a portfolio.

Desirable

  • Awareness of the roles of Ethics, HRA, R&D legislation, and the consent process in clinical research.