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    Training Data - Leeds, United Kingdom - Leeds Teaching Hospitals NHS Trust

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    Description
    data management of clinical trials supporting and facilitating both academic and

    commercial clinical trials alongside a lead research nurse. and Quality Assurance are key aspects of this post. and close down of all clinical trials within their portfolio. for coordination of clinical trials, for the team, and also have a role in recruiting

    patients into clinical trials ensuring that all trial protocols are adhered to.

    Excellent IT skills with a working knowledge of Microsoft

    Office software are essential. Clinical Trials support is provided to a number

    expanding clinical trials department where the trials portfolio includes national

    and specialist group studies plus studies from the commercial sector. will be expected to support the Senior Research Nurse/Midwife/Allied Health

    They will undertake regular auditing/monitoring to ensure that

    research complies with the UK Policy Framework for Health and Social Care

    The post holder will be required to work alongside academic and industry

    partners, the National Institute for Health Research (NIHR) Clinical Research

    Network (CRN) Yorkshire and Humber (Y& H) and colleagues in neighbouring

    Research is at the heart of our Trust. Leeds Teaching Hospitals is involved in research at all levels, developing and trialling new treatments for patients. We believe that being involved in cutting-edge research helps us provide better care to our patients.


    Over the next 5 years, we aim to be the best Trust to deliver high-quality clinical research and to champion research amongst our staff.

    We also aim to support and grow our world-class clinical infrastructure and assets for research and innovation.

    Be the best Trust to deliver high-quality Clinical Research

    Be the Best NHS Trust to Champion Research

    And to maintain and grow world-class clinical infrastructure and assets for research and innovation.

    We have a very proactive Research Academy.

    It offers an extensive programme of education and training tailored to meet the needs of individuals, teams involved in clinical research delivery in Health and Social Care.


    Leeds Teaching Hospitals is committed to our process of redeploying 'at risk' members of our existing workforce to new roles.

    As such, all our job adverts are subject to this policy and we reserve the right to close, delay or remove adverts while this process is completed.

    data management of clinical trials supporting and facilitating both academic and

    commercial clinical trials alongside a lead research nurse. and Quality Assurance are key aspects of this post. and close down of all clinical trials within their portfolio. for coordination of clinical trials, for the team, and also have a role in recruiting

    patients into clinical trials ensuring that all trial protocols are adhered to.

    Excellent IT skills with a working knowledge of Microsoft

    Office software are essential. Clinical Trials support is provided to a number

    expanding clinical trials department where the trials portfolio includes national

    and specialist group studies plus studies from the commercial sector. will be expected to support the Senior Research Nurse/Midwife/Allied Health

    They will undertake regular auditing/monitoring to ensure that

    research complies with the UK Policy Framework for Health and Social Care

    The post holder will be required to work alongside academic and industry

    partners, the National Institute for Health Research (NIHR) Clinical Research

    Network (CRN) Yorkshire and Humber (Y& H) and colleagues in neighbouring

    Proactive and flexible approach, able to work Commitment to personal development
    Knowledge of data protection issues

    Experience in negotiating clinical trials costs
    Clinical research qualification

    Working knowledge of and experience in the effective use of Microsoft Office software including Excel and PowerPoint
    Good Clinical Practice (GCP) training
    Able to fulfil Occupational Health requirements for the post (with reasonable adjustments if necessary), including clearance on blood borne viruses in compliance with Trust Policy

    Experience within a clinical trials setting.
    Experience of data and project management
    Experience of clinical trials co-ordination

    Experience of monitoring clinical trials


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