Clinical Research Nurse

Job overview

Band 6 - Clinical Research Nurse

The Research and Development Department is looking for an experienced nurse with venepuncture and cannulation skills to be in charge and coordinate a portfolio of studies of all types and phases to include complex and early phase studies. On a daily basis the post holder will be responsible for all aspects of the research process including: assessing patient suitability for trials, screening and recruiting patients; obtaining informed consent, performing study procedures to include venepuncture and cannulation and managing study data. A key aspect of this role is supporting the patient / participant and their family throughout the above research process.

You will be part of the friendly, dynamic and supportive team, helping to support the delivery of high quality NIHR portfolio and commercial research, from initiation to termination, in accordance with ICH Good Clinical Practice guidelines.

It is also essential that you can plan and prioritise your workload in order to meet performance targets and deadlines. In order to experience a rewarding career in research we will support you to reach your fullest potential.

Main duties of the job

Lead, coordinate and /or work as a member of the team on studies of all types and phases to include complex and early phase studies. Lead, coordinate and /or work as a member of the team on larger studies e.g. vaccine trials. Recruit and obtain informed consent from participants for non-CTIMP studies (i.e. observational and questionnaire) as delegated by Principal Investigator (PI) and within parameters of the protocol. Support participants considering taking part in interventional and observational research with the decision-making process, ensuring that their information needs are met sensitively and that they have a full understanding of the research study and its requirements. The key elements of our R&D strategy include: to increase the number of UK CRN portfolio and commercial studies, increase patient participation in clinical studies and ensure that studies recruit to time and target. You will work under the management of the Team Leader and Lead Research Nurse, but will need to have excellent organizational skills. It is also essential that you can plan and prioritize your workload in order to meet performance targets and deadlines. In order to experience a rewarding career in research we will support you to reach your full potential and we would encourage you to take advantage of the many opportunities for self-development.

Detailed job description and main responsibilities

Clinical Trial Management (CTIMPs and Non-CTIMPs)

• Obtain informed consent from participants for non-CTIMP studies (i.e. observational and questionnaire) as instructed by Principal Investigator (PI) and within parameters of the protocol.
• Support participants considering taking part in interventional and observational research with the decision-making process, ensuring that their information needs are met sensitively and that they have a full understanding of the research study and its requirements.
• To ensure all Adverse Events are reported in line with the Trust Adverse Events Reporting policy
• Ensuring all reporting to regulatory bodies and Research Networks (if applicable) is done in a timely manner.
• Facilitate and maintain (written and verbal) communication between the PI, research and clinical teams in ensuring that the study protocol is correctly implemented and research governance standards are met and maintained.
• Ensuring that all equipment used in the trial is appropriately calibrated and that supporting documentation is retained.
• Perform all visits, observations, and clinical procedures such as monitoring vital signs, body measurements, height and weight, ECGs, venipuncture, cannulation, drug administration with the participants in accordance with the procedures and schedule of the study protocol.
• Undertake laboratory work as per study protocols, including processing, packaging, storing and transportation of samples.
• Provide ongoing support to patients and volunteers with regards to their trial participation.
• Ensure that all clinical trial databases and logs are maintained including updating patient recruitment data on EDGE, our Local Performance Management System, on a weekly basis.
• Ensure protocol amendments are incorporated into research practice in a timely manner.
• Work within the scope of research guidelines, ethical principles and protocols, whilst adhering to organisational policies and procedures.
• Adhere to the confidentiality of patient information at all times, in accordance with the Data Protection Act and Caldicott regulation

For more information please see Job Description

Applicant requirements

You must have appropriate UK professional registration.

This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service.