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An exciting opportunity for a Band 6 Research Midwife at a leading NHS Trust. The role involves managing clinical trial caseloads, supporting patients, and collaborating with a multidisciplinary team. Previous clinical research experience is desirable but training is available. Join a dynamic and innovative environment dedicated to exceptional care.
An opportunity has arisen for a Band 6 Research Midwife to join our research delivery team to support the growing portfolio of research studies undertaken by the research team at UHDB. The post will suit a dynamic, enthusiastic and creative individuals looking to further their career in research.
The post holder will be working with a renowned multidisciplinary team in various areas. You will manage your own caseload of patients on clinical trials with the support of the wider research and clinical team.
You will be expected to deputise in the absence of the Senior Research Midwife as required. Previous clinical research experience with drug and commercial trials is desirable, however training is offered.
Preferably educated to degree level or equivalent, you will work within the guidelines and policies for the conduct of clinical trials, ensuring high standards of practice in accordance with the principles of GCP.
The successful applicant should have a flexible approach and the ability to work both as part of the team and independently. In addition, excellent communication, administrative and IT skills and being supportive and open to new initiatives are valued by the team.
The post holder will support trials from set up to close and will be responsible for assessing and managing the care pathways for patients and carers participating in clinical trials. This will involve the recruitment, education and monitoring of research participants and the collection and documentation of accurate data.
You will be working closely with principal investigators and members of the multidisciplinary team, and will support patients who choose to participate in clinical trials by providing advice and information and acting as the patients' advocate.
An important aspect of the role is the maintenance of accurate and comprehensive records of data derived from the research studies. The post holder will be involved in ensuring that any research undertaken within the department safeguards the well-being of the patients and is conducted within ICH Good Clinical Practice Guidelines for Research.
You will have an excellent range of clinical skills and can demonstrate significant knowledge and some experience of supporting clinical research in a hospital setting.
Proven recent experience of coordinating/supporting complex research studies and using the study intensity tool to manage workload is required for the post.
You will be an effective communicator who can work well both independently and within a multi-disciplinary team, with excellent attention to detail.
Closing date of applications: 9 July 2025
Interview date: 23 July 2025
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