PRAHS

  • Clinical Trial Assistant

    Job Locations - | China
    Posted Date 2 weeks ago(5/8/2018 12:57 AM)
    ID
    2018-46752
  • Overview

    As a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs.

    At PRA Health Sciences, providing innovative solutions for our clients is what we do. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.

    At PRA, borders do not create boundaries.  PRA’s success is dependent upon our ability to attract and retain a talented team of diverse professionals.  Our growing workforce is comprised of over 10,000 employees, spanning 13 time zones across six continents and who speak more than 30 languages – yet operate in unison as one worldwide PRA community. 

    Responsibilities

    Providing innovative solutions for our clients is what we do. But innovation just for the sake of innovation isn’t why we do it. Side-by-side with our clients, we strive to move drug discovery forward, to help them develop lifesaving and life-improving drugs. We help change people’s lives for the better every single day. It’s who we are. And it’s who you could be too. Working fully embedded within one of our pharmaceutical clients, with the support of PRA right behind you, you’ll be at the heart of our client’s innovation.

     

     

    Position Overview:

     

    Working fully embedded within the local clinical team at our client’s offices, the Clinical Trial Assistant plays a key role in the success of global clinical trials at a local level. The tasks undertaken by a CTA are varied and can include:

     

    • Providing ongoing administrative support to other members of the clinical study team, supporting other clinical colleagues in tracking study progress
    • Collaborating with site staff to ensure clinical trials are being run according to the protocol 
    • Document management, tracking, electronic filing and review
    • Ensuring studies are run according to ICH GCP and other applicable regulations at site
    • Organising meetings
    • Managing the delivery of non-drug related study supplies
    • Supporting the study start up process locally

     

    As a Clinical Trial Assistant, you will have the opportunity to experience the full lifecycle of a project and genuinely contribute to drug development and improving patients’ lives.

     

    Qualifications

    You are: 

     

    Detail-orientated, passionate and reliable.

     

    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:

     

    • A relevant educational background, either in life-sciences or as a licensed healthcare professional
    • Strong interpersonal skills
    • Proficiency in MS Office
    • The ability to manage multiple priorities simultaneously
    • A quality-focused mindset

     

    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.

     

    PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.

     

     

    For more information please visit our website: www.prahs.com

     

     

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