Clinical Trials Administrator

2 weeks ago


Preston, United Kingdom Lancashire Teaching Hospitals NHS Foundation Trust Full time

We are delighted to offer within the Research & Innovation Department, working in Clinical Research as a Clinical Trials Administrator (CTA).

You will be working closely with the Cancer Research Nurses, inputting clinical data and assisting with the general running of clinical trials on a day to day basis.

With your help we can improve healthcare through research and innovation.

Knowledge and understanding of NHS systems and clinical research is not essential, as you will be provided with training, but it is desirable. You will also need excellent computer skills to handle the multitude of electronic systems associated with clinical trials.

Great administration and communication skills are required too, as well as being able to prioritise your workload and work autonomously when required to.

We are committed to leading improvements in healthcare through research and innovation. The Centre for Health Research and Innovation is a dynamic environment for the support and development of health research, innovation and clinical trials. We employ a large multi-disciplinary team of enthusiastic and committed staff who work alongside the health care teams to offer our patients the opportunity to be involved in research.

You will work in close partnership with the local Clinical Research Networks and together we have developed a broad portfolio of high quality research. We are excited to be strengthening our academic and industry links and building on the success of our existing programme of original research.

As a member of our team you will have access to high quality training and continued professional development. You will be part of a supportive team with the opportunity to develop your knowledge and skills. You will be provided with a comprehensive induction programme and have a personal development plan tailored to your training and development needs.

You will be providing support with set up and management of clinical trials will be a key part of this role, and you will be able to demonstrate attention to detail, organisational and computer skills, as the role would require regular data management and some clerical work.

You will have a flexible approach and be able to balance competing demands through effective prioritisation and excellent communication skills.

For the full description, please see the document attached.


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