PRAHS

  • In-house Clinical Research Associate

    Job Locations - | Taiwan
    Posted Date 3 weeks ago(3 weeks ago)
    ID
    2018-49011
  • Overview

    In-House Clinical Research Associate

    Location (Taipei, Taiwan)

     

    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.

    Responsibilities

    As an In-house Clinical Research Associate you will be working closely with the wider project team to support the management of investigative sites and ensure that all sites adhere to the requirements and regulations governing Clinical Research. You will receive comprehensive training which will enable you to learn, before moving to work on your own studies with continuing support, training and mentorship.

     

    You will have the opportunity to work on clinical studies at different stages of the project lifecycle and gain a variety of therapeutic experience. The In-house Clinical Research Associate supports with feasibility, study start-up, assisting sites during maintenance and closing out sites.

     

    Key responsibilities in this position include:

    • Demonstrates good working knowledge of PRA systems and work environment
    • Demonstrates thorough knowledge of finance background for site contracts and payment.
    • Exhibits good decision making skills utilizing all available resources for determining positive outcomes.
    • Successfully interacts with both internal and external customers, representing the organization on specific projects.

    Qualifications

    In addition to above:

    • Minimum of 2 years of related experience (site contract & payment)
    • Experience with PC-Windows, word processing, and electronic spreadsheets required.
    • Knowledge of ICH and local regulatory authority drug research and development regulations required.
    • Clinical trials support or pharmaceutical industry experience required.
    • Experience leading a team in a clinical research environment preferred.


    PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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