The position offers opportunities for training and the potential to gain accreditation as a Clinical Research Practitioner. The successful candidate will work within a supportive team environment, engaging with various professional groups and research sponsors. The role plays a vital part in expanding the clinical trials portfolio, which spans phases 1-4 and includes both interventional and non-interventional studies.
An exciting opportunity has arisen within the developing Clinical Research Unit at the Bristol Eye Hospital. We are looking to appoint an enthusiastic individual as a Clinical Trial Co-ordinator.
In this position you will work closely with members of a multi-disciplinary research team to provide them with clinical and administrative support for a portfolio of clinical trials.
The work requires initiative, accuracy and attention to detail. Experience of clinical research projects within the NHS or academic/commercial settings will be essential. You will be in contact with a broad professional group, as well as members of the public and research sponsors therefore excellent communication, interpersonal and organisational skills will be of equal importance.
Experience in clinical research is required and ophthalmology experience would be advantageous.
You will be performing a variety of duties within this position. This will include setting up trials, working closely with the Trust R&I department to gain the necessary approvals.
You will manage an ongoing portfolio of studies, performing a variety of tasks such as completing case report forms, maintaining study documentation, processing amendments, and planning and organising patient appointments.
A component of this role is the requirement to perform some clinical work, for example, including assisting in the informed consent procedure, venepuncture, vital signs, urine testing and ECGs. Full training will be given, with an opportunity to gain accreditation as a Clinical Research Practitioner, which is now identified as an occupational group in health and care in the UK by the UK Professional Standards Authority (PSA).
Training and development features high on our list of priorities. Therefore the post holder will be a flexible, motivated team player willing to further develop their understanding of clinical trials.
About us
You will be working as part of our friendly and supportive team. Our clinical trials portfolio covers the full spectrum of phase 1-4 studies and incorporates both interventional and non-interventional studies. As well as being part of our BEH CRU team, you will be working with our pharmaceutical and non-commercial sponsors, helping us to develop these relationships to enable future growth of our service and subsequently more choice for our patients. We have been the highest recruiting site in the UK for 15+ studies since 2, a track record that has been achieved through close alliance between our research staff and clinical services.
For a more detailed job description, main responsibilities, and person specification, please refer to the job description document attached to this vacancy.
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