• Senior Clinical Data Coordinator

    Job Locations (All) | United Kingdom | United Kingdom-London
    Posted Date 1 week ago(1/7/2019 4:20 AM)
  • Overview

    PRA Health Sciences is an award winning CRO.


    We are proud to have won Pharma Times 'Clinical Research Company of the Year' in 2017 for the fourth consecutive year. We aren’t winning these awards by chance; PRA is being recognised industry-wide for our dedication to the future of clinical development. Most importantly for you, at PRA we recognise that our success is down to our people.


    As a Senior Clinical Data Coordinator you will be dedicated to one of our global pharmaceutical clients; a prestigious organization, specialising in a niche rare disease, complemented by a pipeline in other therapeutic areas, including oncology. A company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. 

    You will work from the clients' offices in London, with some flexibility to work from home. 



    The Senior Clinical Data Coordinator performs basic and mid-level data management tasks independently and complex tasks under supervision of the Lead Data Manager, and may oversee multiple small scope studies.

    Key responsibilities in this role include:


    • Designs CRF’s or eCRF’s, with input from cross functional study team
    • Develops edit check specifications, data management plans, data review guidelines and SAE reconciliation plan
    • Oversees vendor Data Management activities
    • Communicate quality control results and identify and resolve systematic issues.
    • Ability to communicate project issues at both a summary and detail level to Lead Data Managers (LDM) and functional management.
    • Completion of quality control steps.
    • Following database closure procedures for freezing, locking, and unlocking clinical databases.


    You are:


    Detail focused, adaptable and a communicative leader


    Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:

    • Degree qualified with demonstrable experience working within a CRO and or pharmaceutical industry
    • Proficiency in at least one Clinical Data Management system required
    • Experience working in industry standard Clinical Data Management system(s)
    • Experience with all steps within the Data Management lifecycle
    • Experience as primary representative of Clinical Data Management project team
    • Communication skills and an ability to quickly build relationships


    Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better.


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