• Clinical Trial Assistant (CTA) for Contracts- office based in Barcelona (mat leave)

    Job Locations (All) | Spain-Barcelona
    Posted Date 2 weeks ago(10/10/2018 12:01 PM)
  • Overview

    At PRA, we don’t make our 15000+ people great. It’s the other way around. As we have grown to a top-5 CRO, we have maintained the feel of a small company, dedicated to collaboration and passion for what we do.


    We always have a desire to keep seeking new and better ways to operate. We don’t settle for the same old ways. Our passion for improving patient lives worldwide permeates all that we do. Put simply, we care.



    We are looking for a Clinical Trial Assistant for Contracts based in Barcelona to cover a maternity leave.


    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.


    As a Clinical Trial Assistant, you will be dedicated to one of our global pharmaceutical client; with whom PRA shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in this exclusive program.


    The Clinical Trial Assistant plays a fundamental role in the successful execution of global clinical trials by supporting the Local Study Team and being responsible for the relationship with sites involved in clinical trials including work from contract and amendment language, budget negotiation within the established timeline parameters.


    Key responsibilities in this role include:


    - Receiving requests for contracts and responding within expected turnaround time


    - Initiating and following processes for managing contracts 


    - Tracks and timely records developments 


    - Managing documents from creation to completion


    - Maintaining status reports on all activities



    Highly organised, a problem solver and detail driven.


    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:


    • Experience in a similar role in the pharmaceutical / clinical research industry.
    • The ability to manage multiple priorities simultaneously
    • Excellent negotiation skills
    • A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
    • Fluent English and Spanish, along with proficiency in the use of Microsoft Office suite


    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:


    Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
    Share on your newsfeed

    Connect With Us!

    Not ready to apply? We get it! Click here to stay in touch for future opportunities, events and other happenings!