Detailed job description and main responsibilities

The job description outlines the core requirements expected of a Research Nurse. The list is not exhaustive and specific requirements related to any specialist area of practice will be outlined with the prospective post holder. These will be included as an addition to these generic descriptors as role specific prior to employment together with the professional development plans. 

The post holder will practice with knowledge, skills and behaviours which…

·         Manage workload and co-ordinate allocated clinical trials and research studies. 

·         Practice in compliance with their code of professional conduct, being responsible and accountable for their decisions, actions, or omissions.

·         Utilise effective communication skills through a variety of methods, supporting participants in decision making in relation to clinical trial and study entry and participation.

·         Utilise effective communication skills with colleagues both internally and/or externally, in verbal, non-verbal and written communication methods, adapting to changing parameters as required, which includes thorough accurate documentation in patient records as required.

·         Provide and receive highly sensitive, complex, or contentious information relating to participant involvement and care, and communicates information to participants, families or carers with respect, compassion, and empathy.

·         Able to competently perform a range of clinical procedures as required as part of the research protocol, ensuring accurate data capture.

·         Administer systemic anticancer therapies including novel agents, according to trial protocols as required. Ensure patients and relatives are taught the correct method of administration, where appropriate.

·         Identify and discuss patient needs with the research team, patients, carers, and the multi- disciplinary team. Participate in decision making concerning treatment of patients on clinical trials in accordance with the trial protocol.

·         Develop and maintain skills including cannulation, phlebotomy, central venous line care, intravenous drug administration, and systemic anticancer therapies competencies as necessary.

·         Participate in and ensure compliance with Informed Consent Procedures, acting within boundaries of own competency, research regulation and Trust policies/SOPs.

·         Use own professional judgment identifying when to escalate and seek senior support/guidance.

·         Support the research team with all administrative tasks, including study set up including completion of feasibility requests, as required.

·         Ensure all necessary regulatory approvals are in place prior to approaching potential study participants.

·         Work within the limits of the approved protocol and any approved amendments.

·         Identify suitable patients for entry into clinical trials by attending clinics and relevant Multi-disciplinary Team meetings, using relevant clinical knowledge to identify patients suitable for clinical research using inclusion and exclusion criteria and utilising NHS records, visiting wards and outpatients where appropriate.

·         Communicate complex and sensitive information effectively to patients, carers, and other staff, overcoming barriers to understanding and providing support during distressing or emotional events.

·         Participate in the recording of information into Case Report Forms and resolving data queries. Meet with Clinical Research Associates routinely during monitoring visits and respond to follow up letters as required.