PRAHS

  • Clinical Research Associate - 1 year contract

    Job Locations - | Turkey
    Posted Date 7 days ago(7/10/2018 5:26 AM)
    ID
    2018-47864
  • Overview

    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 life-saving 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.

    Responsibilities

    As a Clinical Research Associate you will be dedicated to one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies and vaccines for many of the world’s most challenging diseases including cancer, cardio-metabolic diseases, Alzheimer’s and infectious diseases. Be ready to work in a solid partnership and an environment driven by innovation and continuous improvement. 

    Typical responsibilities:

    • Monitoring of clinical trials according to ICH-GCP standards
    • Development and review of documentation related to clinical trials
    • Development of study protocol design
    • Document management related to regulatory and ethical committee approvals
    • Performing pre-study initiation, interim monitoring and close out visits
    • Review of drug shipment and drug accountability
    • Organanising and attending investigator meetings as required
    • Providing the support to the Project Manager with other tasks as required

     

    As a Clinical Research Associate, 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: Well organised, flexible and have fantastic communication skills 

    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:

     

    • Strong understanding of ICH-GCP
    • 6 + months of experience in monitoring of clinical trials
    • Strong organisational skills
    • A quality-focused mindset
    • Bachelor’s degree or Master’s degree or equivalent / PhD or MD
    • Fluency in written and spoken Turkish and English

     

    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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