• In-House CRA

    Job Locations (All) | Spain-Madrid
    Posted Date 1 week ago(12/7/2018 4:37 AM)
  • 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 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. 



    The In-House CRA plays an integral role in our clients Global Clinical Services function supporting the trial management and operational activities of assigned clinical studies. We currently have an opening for an In-House CRA to join our team in Spain.


    Role responsibilities include:


    • Lead and participate in key Clinical Operations activities associated with initiation, maintenance, and closure of clinical studies and individual investigative sites with close supervision from the Project Manager
    • Lead Trial Master File (TMF) activities including oversight of partners and ongoing inspection/audit readiness
    • Anticipates, identifies, and communicates with Line Manager/Project Manager any issues that could affect timelines and works to develop alternative solutions.
    • Participate in the creation, review and maintenance of Clinical Project Documents in partnership with the relevant groups and team members
    • Support Project Manager with meetings including agenda preparation, material distribution, minutes and action item follow-up


    You are:


    Analytical and conceptual with a high attention to detail, you should be able to communicate at a cross functional level demonstrating negotiation and persuasion 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:

    • A Bachelor’s Degree with a minimum two years’ experience in the pharmaceutical industry, supporting clinical study conduct in an operational or training capacity
    • Thorough knowledge of the operational aspects of pharmaceutical studies
    • Demonstrated analytical and conceptual capability
    • Knowledge of GCP and relevant regulations that govern essential documents
    • Advanced organizational and communication skills
    • Attention to detail
    • Teamwork and motivational skills                                                    

    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.


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